Transcript #00009266 (NM_004667.5, HERC2 gene)

Transcript name HECT and RLD domain containing E3 ubiquitin protein ligase 2
Gene name HERC2 (HECT and RLD domain containing E3 ubiquitin protein ligase 2)
Chromosome 15
Transcript - NCBI ID NM_004667.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_004658.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

231 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-31G>A r.(?) p.(=)
+/. 56i_93_ c.8826-1802_*726{0} r.? p.?
-?/. - c.187+7G>A r.(=) p.(=)
?/. - c.233A>G r.(?) p.(Asp78Gly)
?/. - c.293T>C r.(?) p.(Leu98Pro)
?/. - c.293T>C r.(?) p.(Leu98Pro)
?/. - c.293T>C r.(?) p.(Leu98Pro)
?/. - c.293T>C r.(?) p.(Leu98Pro)
-?/. - c.326T>C r.(?) p.(Val109Ala)
?/. - c.547C>T r.(?) p.(Arg183Trp)
-?/. - c.643+5G>A r.spl? p.?
-?/. - c.643+8C>T r.(=) p.(=)
-?/. - c.738G>A r.(?) p.(Val246=)
-?/. - c.836del r.(?) p.(Gly279Glufs*25)
-?/. - c.905C>T r.(?) p.(Thr302Met)
-?/. - c.1012T>G r.(?) p.(Leu338Val)
-?/. - c.1015C>T r.(?) p.(Pro339Ser)
?/. - c.1015C>T r.(?) p.(Pro339Ser)
-/. - c.1083C>T r.(?) p.(His361=)
?/. - c.1150G>A r.(?) p.(Glu384Lys)
?/. - c.1403G>A r.(?) p.(Arg468His)
-?/. - c.1731C>T r.(?) p.(Arg577=)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/. - c.1781C>T r.(?) p.(Pro594Leu)
+/? 14 c.1781C>T r.1781c>u p.Pro594Leu
-?/. - c.1794C>T r.(?) p.(Ala598=)
?/. - c.2030A>G r.(?) p.(Gln677Arg)
-?/. - c.2317-3T>C r.spl? p.?
-?/. - c.2379_2382delinsTATT r.(?) p.(=)
?/. - c.2382C>T r.(?) p.(=)
-/. - c.2389A>G r.(?) p.(Met797Val)
-?/. - c.2389A>G r.(?) p.(Met797Val)
-/. - c.2448C>T r.(?) p.(Ser816=)
?/. - c.2747-3C>A r.spl? p.?
?/. - c.2766C>G r.(?) p.(Asn922Lys)
-?/. - c.3140G>A r.(?) p.(Arg1047Lys)
?/. - c.3260C>A r.(?) p.(Ser1087Tyr)
?/. - c.3705A>G r.(?) p.(Ile1235Met)
?/. - c.3763G>A r.(?) p.(Glu1255Lys)
-/. - c.3903T>A r.(?) p.(Pro1301=)
-/. - c.4009C>T r.(?) p.(Leu1337Phe)
+?/. - c.4126C>T r.(?) p.(Arg1376Ter)
?/. - c.4145G>A r.(?) p.(Arg1382Gln)
?/. - c.4235T>C r.(?) p.(Ile1412Thr)
?/. - c.4309G>C r.(?) p.(Gly1437Arg)
-?/. - c.4605A>G r.(?) p.(Lys1535=)
+/. - c.4625G>A r.(?) p.(Arg1542His)
+/. - c.4625G>A r.(?) p.(Arg1542His)
-?/. - c.4625G>A r.(?) p.(Arg1542His)
?/. - c.4651A>C r.(?) p.(Ile1551Leu)
?/. - c.4651A>C r.(?) p.(Ile1551Leu)
+?/. - c.4676-1G>A r.spl? p.?
?/. - c.4723G>A r.(?) p.(Glu1575Lys)
?/. - c.4742_4744del r.(?) p.(Glu1581del)
-?/. - c.4809+3G>C r.spl? p.?
?/. - c.4892C>T r.(?) p.(Pro1631Leu)
-?/. - c.5040C>G r.(?) p.(Ser1680Arg)
?/. - c.5057C>T r.(?) p.(Pro1686Leu)
?/. - c.5213G>C r.(?) p.(Trp1738Ser)
?/. - c.5213G>C r.(?) p.(Trp1738Ser)
-?/. - c.5315C>T r.(?) p.(Pro1772Leu)
-?/. - c.5391C>T r.(?) p.(His1797=)
-?/. - c.5429T>C r.(?) p.(Met1810Thr)
-?/. - c.5440A>G r.(?) p.(Thr1814Ala)
-?/. - c.5442G>T r.(?) p.(Thr1814=)
-?/. - c.5566C>T r.(?) p.(Leu1856Phe)
-/. - c.5577A>T r.(?) p.(Ser1859=)
?/. - c.5588T>C r.(?) p.(Leu1863Pro)
-?/. - c.5596A>G r.(?) p.(Met1866Val)
?/. - c.5654A>G r.(?) p.(Asp1885Gly)
-?/. - c.5799T>A r.(?) p.(Ala1933=)
-?/. - c.5809C>T r.(?) p.(Pro1937Ser)
?/. - c.5825C>T r.(?) p.(Ser1942Leu)
-?/. - c.5926C>T r.(?) p.(Leu1976=)
?/. - c.6077C>T r.(?) p.(Thr2026Met)
?/. - c.6110C>T r.(?) p.(Pro2037Leu)
-?/. - c.6123C>T r.(?) p.(Gly2041=)
-?/. - c.6195C>T r.(?) p.(Thr2065=)
-?/. - c.6261C>T r.(?) p.(Thr2087=)
?/. - c.6385C>T r.(?) p.(Arg2129Cys)
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