Transcript #00009460 (NM_031935.2, HMCN1 gene)

Transcript name hemicentin 1
Gene name HMCN1 (hemicentin 1)
Chromosome 1
Transcript - NCBI ID NM_031935.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_114141.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.114G>T r.(?) p.(Gly38=)
-?/. - c.114G>T r.(?) p.(Gly38=)
-?/. - c.437G>A r.(?) p.(Arg146Gln)
+?/. - c.601G>A r.(?) p.(Asp201Asn)
-?/. - c.602A>G r.(?) p.(Asp201Gly)
-?/. - c.669T>A r.(?) p.(Leu223=)
-?/. - c.785A>G r.(?) p.(Asn262Ser)
-?/. - c.861G>A r.(?) p.(Val287=)
-?/. - c.901-15A>G r.(=) p.(=)
?/. - c.1015G>A r.(?) p.(Val339Met)
?/. - c.1239C>A r.(?) p.(Tyr413Ter)
-/. - c.1266C>G r.(?) p.(Ser422=)
-?/. - c.1338G>C r.(?) p.(Pro446=)
-?/. 10 c.1535C>T r.(?) p.(Thr512Ile)
?/. - c.1535C>T r.(?) p.(Thr512Ile)
?/. - c.1535C>T r.(?) p.(Thr512Ile)
-?/. - c.1637C>T r.(?) p.(Ala546Val)
?/. - c.2119G>T r.(?) p.(Val707Phe)
-?/. - c.2157C>T r.(?) p.(Thr719=)
-?/. - c.2164G>A r.(?) p.(Glu722Lys)
-?/. - c.2212+8T>G r.(=) p.(=)
-?/. - c.2372-3C>T r.spl? p.?
?/. 16 c.2420G>A r.(?) p.(Gly807Asp)
?/. - c.2437C>T r.(?) p.(Pro813Ser)
-?/. - c.2559T>C r.(?) p.(=)
?/. - c.2767C>T r.(?) p.(Arg923Trp)
-?/. - c.3166A>G r.(?) p.(Thr1056Ala)
-?/. - c.3166A>G r.(?) p.(Thr1056Ala)
-?/. - c.3236G>A r.(?) p.(Arg1079Gln)
?/. - c.3262G>A r.(?) p.(Glu1088Lys)
-?/. - c.3300A>G r.(?) p.(Pro1100=)
-?/. - c.3307G>A r.(?) p.(Val1103Met)
?/. - c.3310A>G r.(?) p.(Lys1104Glu)
-?/. - c.3377+14dup r.(=) p.(=)
?/. 23 c.3498T>G r.(?) p.(Asn1166Lys)
?/. - c.3553G>T r.(?) p.(Gly1185Cys)
-?/. 24 c.3695C>T r.(?) p.(Thr1232Met)
-?/. - c.3695C>T r.(?) p.(Thr1232Met)
?/. - c.4009A>T r.(?) p.(Ile1337Phe)
?/. - c.4112C>T r.(?) p.(Ser1371Leu)
+/. - c.4163del r.(?) p.(Pro1388Hisfs*14)
-?/. - c.4269A>G r.(?) p.(Pro1423=)
?/. - c.4337T>C r.(?) p.(Ile1446Thr)
-?/. - c.4373A>G r.(?) p.(Asn1458Ser)
?/. - c.4468G>A r.(?) p.(Asp1490Asn)
-?/. - c.4515C>G r.(?) p.(Asp1505Glu)
-/. - c.4515C>G r.(?) p.(Asp1505Glu)
?/. - c.4547G>A r.(?) p.(Arg1516Gln)
?/. - c.4547G>A r.(?) p.(Arg1516Gln)
?/. - c.4547G>A r.(?) p.(Arg1516Gln)
-?/. 30 c.4586A>G r.(?) p.(Asn1529Ser)
-?/. - c.4586A>G r.(?) p.(Asn1529Ser)
-?/. - c.4586A>G r.(?) p.(Asn1529Ser)
?/. - c.4667A>G r.(?) p.(Asp1556Gly)
-?/. - c.4782A>G r.(?) p.(=)
-?/. - c.4910-14A>G r.(=) p.(=)
-?/. - c.4910-14_4910-13del r.(=) p.(=)
-?/. - c.4998T>C r.(?) p.(Ala1666=)
-?/. - c.4998T>C r.(?) p.(Ala1666=)
-?/. - c.5014A>G r.(?) p.(Ile1672Val)
-?/. - c.5070A>T r.(?) p.(Ile1690=)
-?/. - c.5070A>T r.(?) p.(Ile1690=)
-?/. - c.5395A>G r.(?) p.(Asn1799Asp)
?/. - c.5474C>T r.(?) p.(Pro1825Leu)
+?/. 35 c.5482A>G r.(?) p.(Ile1828Val)
-/. - c.5851+10del r.(=) p.(=)
-?/. - c.5851+10del r.(=) p.(=)
?/. - c.5881C>T r.(?) p.(Leu1961Phe)
-?/. - c.6029-11G>T r.(=) p.(=)
-?/. - c.6029-4T>C r.spl? p.?
-?/. - c.6029-4T>C r.spl? p.?
-?/. - c.6029-4T>C r.spl? p.?
?/. - c.6089G>A r.(?) p.(Arg2030Lys)
-?/. - c.6150T>C r.(?) p.(Ser2050=)
-?/. - c.6181-17G>A r.(=) p.(=)
-?/. - c.6287T>A r.(?) p.(Ile2096Asn)
-?/. - c.6305-16C>T r.(=) p.(=)
?/. - c.6511C>T r.(?) p.(Arg2171Cys)
-?/. - c.6701-18A>G r.(=) p.(=)
-?/. - c.6708A>G r.(?) p.(Pro2236=)
?/. - c.6812C>T r.(?) p.(Ala2271Val)
-?/. 45 c.6981G>A r.(?) p.(Met2327Ile)
-?/. - c.6981G>A r.(?) p.(Met2327Ile)
?/. - c.7048C>A r.(?) p.(Leu2350Met)
?/. - c.7079G>A r.(?) p.(Arg2360His)
?/. - c.7144+1G>A r.spl? p.?
-?/. - c.7426+10T>G r.(=) p.(=)
-?/. 48 c.7477G>C r.(?) p.(Glu2493Gln)
-?/. - c.7494G>A r.(?) p.(Thr2498=)
-?/. - c.7555C>G r.(?) p.(Pro2519Ala)
-?/. - c.7652T>C r.(?) p.(Leu2551Ser)
?/. - c.7652T>C r.(?) p.(Leu2551Ser)
+/. - c.7677G>C r.(?) p.(Lys2559Asn)
-?/. - c.7705+4G>A r.spl? p.?
-?/. - c.7706-9C>T r.(=) p.(=)
-?/. - c.7818C>T r.(?) p.(=)
-?/. - c.8028G>A r.(?) p.(Gly2676=)
-?/. - c.8094G>A r.(?) p.(=)
?/. 53 c.8150C>T r.(?) p.(Ser2717Phe)
-?/. - c.8174C>T r.(?) p.(Ala2725Val)
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