Transcript #00009265 (NM_003922.3, HERC1 gene)

Transcript name HECT and RLD domain containing E3 ubiquitin protein ligase family member 1
Gene name HERC1 (HECT and RLD domain containing E3 ubiquitin protein ligase family member 1)
Chromosome 15
Transcript - NCBI ID NM_003922.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_003913.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

140 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.228C>G r.(?) p.(Asp76Glu)
?/. - c.260T>A r.(?) p.(Leu87Gln)
-?/. - c.300C>T r.(?) p.(Ala100=)
?/. - c.527G>A r.(?) p.(Ser176Asn)
-?/. - c.570C>T r.(?) p.(Asn190=)
-/. - c.570C>T r.(?) p.(Asn190=)
-?/. - c.621A>G r.(?) p.(Ser207=)
-?/. - c.780A>G r.(?) p.(Ser260=)
-?/. - c.786A>G r.(?) p.(Arg262=)
?/. - c.827C>A r.(?) p.(Ala276Glu)
-?/. - c.999C>T r.(?) p.(Tyr333=)
-/. - c.1101T>C r.(?) p.(Ile367=)
-?/. - c.1128T>C r.(?) p.(Val376=)
?/. - c.1715A>T r.(?) p.(His572Leu)
-?/. - c.1988C>G r.(?) p.(Ala663Gly)
?/. - c.2015T>A r.(?) p.(Ile672Asn)
-?/. - c.2382C>T r.(?) p.(Cys794=)
?/. - c.2455G>T r.(?) p.(Ala819Ser)
?/. - c.2687A>C r.(?) p.(His896Pro)
-?/. - c.2694C>T r.(?) p.(His898=)
-?/. - c.2742A>G r.(?) p.(Leu914=)
-?/. - c.2768A>G r.(?) p.(Asn923Ser)
-?/. - c.2823T>A r.(?) p.(Ala941=)
-?/. - c.2869-5T>C r.spl? p.?
-?/. - c.2871T>C r.(?) p.(=)
-?/. - c.3021+6C>T r.(=) p.(=)
-?/. - c.3113A>C r.(?) p.(Lys1038Thr)
?/. - c.3374G>A r.(?) p.(Gly1125Asp)
?/. - c.3405G>C r.(?) p.(Trp1135Cys)
?/. - c.3451C>T r.(?) p.(Arg1151Trp)
-?/. - c.3565T>C r.(?) p.(Leu1189=)
-/. - c.3565T>C r.(?) p.(Leu1189=)
?/. - c.3721C>G r.(?) p.(Gln1241Glu)
-?/. - c.3870T>G r.(?) p.(=)
?/. - c.3878T>C r.(?) p.(Leu1293Ser)
+?/. - c.3897T>A r.(?) p.(Cys1299*)
?/. - c.4028T>G r.(?) p.(Phe1343Cys)
?/. - c.4028T>G r.(?) p.(Phe1343Cys)
?/. - c.4190G>A r.(?) p.(Arg1397His)
-?/. - c.4232G>T r.(?) p.(Gly1411Val)
-?/. - c.4293T>C r.(?) p.(Leu1431=)
-?/. - c.4323A>G r.(?) p.(Ala1441=)
?/. - c.4457T>A r.(?) p.(Met1486Lys)
?/. - c.4478C>A r.(?) p.(Thr1493Asn)
?/. - c.4483G>A r.(?) p.(Glu1495Lys)
-?/. - c.4714T>G r.(?) p.(Ser1572Ala)
-/. - c.4714T>G r.(?) p.(Ser1572Ala)
-?/. - c.4845T>C r.(?) p.(Ser1615=)
?/. - c.4967G>A r.(?) p.(Ser1656Asn)
-/. - c.5044C>G r.(?) p.(Leu1682Val)
?/. - c.5122G>T r.(?) p.(Asp1708Tyr)
?/. - c.5249A>G r.(?) p.(Gln1750Arg)
-?/. - c.5325C>T r.(?) p.(Ser1775=)
-?/. - c.5481-3T>C r.spl? p.?
-?/. - c.5736C>T r.(?) p.(Arg1912=)
-?/. - c.5791G>A r.(?) p.(Glu1931Lys)
?/. - c.5807T>C r.(?) p.(Ile1936Thr)
-/. - c.5839C>T r.(?) p.(=)
?/. - c.5914G>A r.(?) p.(Val1972Ile)
?/. - c.5914G>A r.(?) p.(Val1972Ile)
-?/. - c.5932G>T r.(?) p.(Ala1978Ser)
-?/. - c.5983A>G r.(?) p.(Thr1995Ala)
?/. - c.6057C>T r.(?) p.(Gly2019=)
-?/. - c.6081T>A r.(?) p.(Asn2027Lys)
?/. - c.6134T>C r.(?) p.(Val2045Ala)
-?/. - c.6195A>G r.(?) p.(Thr2065=)
-?/. - c.6195A>G r.(?) p.(Thr2065=)
-?/. - c.6225+4C>T r.spl? p.?
-?/. - c.6549+5T>C r.spl? p.?
-?/. - c.6549+5T>C r.spl? p.?
?/. - c.6715G>A r.(?) p.(Glu2239Lys)
-?/. - c.6776G>A r.(?) p.(Arg2259His)
?/. - c.6776G>A r.(?) p.(Arg2259His)
-?/. - c.7204G>A r.(?) p.(Val2402Ile)
+?/. - c.7227del r.(?) p.(Ser2410Alafs*29)
-?/. - c.7308C>T r.(?) p.(Ser2436=)
?/. - c.7322G>C r.(?) p.(Arg2441Pro)
?/. - c.7420A>G r.(?) p.(Ser2474Gly)
-?/. - c.7815G>A r.(?) p.(Leu2605=)
-?/. - c.8121A>G r.(?) p.(Leu2707=)
-?/. - c.8199C>T r.(?) p.(Asn2733=)
-?/. - c.8446G>A r.(?) p.(Ala2816Thr)
-?/. - c.8451C>T r.(?) p.(Ala2817=)
-?/. - c.8469G>A r.(?) p.(=)
-?/. - c.8523T>C r.(?) p.(Asp2841=)
-?/. - c.8934G>A r.(?) p.(Val2978=)
?/. - c.9055G>A r.(?) p.(Asp3019Asn)
-?/. - c.9105A>G r.(?) p.(Leu3035=)
-?/. - c.9144C>T r.(?) p.(Thr3048=)
-?/. - c.9438C>T r.(?) p.(Ser3146=)
-?/. - c.9439G>A r.(?) p.(Val3147Ile)
-?/. - c.9455C>T r.(?) p.(Ser3152Phe)
?/. - c.10084+3A>C r.spl? p.?
?/. - c.10358G>A r.(?) p.(Arg3453His)
?/. - c.10454G>A r.(?) p.(Ser3485Asn)
-?/. - c.10458T>A r.(?) p.(Asp3486Glu)
-?/. - c.10547-7C>T r.(=) p.(=)
?/. - c.10572G>C r.(?) p.(Gln3524His)
?/. - c.10586C>A r.(?) p.(Ser3529Tyr)
-?/. - c.10786C>T r.(?) p.(Pro3596Ser)
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