Canonical Allele Identifier: CA645523668

Gene: WFS1

Linked Data

• COSMIC: COSM6100640

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301371_6301372delinsTT , CM000666.2:g.6301371_6301372delinsTT	GRCh38
NC_000004.11:g.6303098_6303099delinsTT , CM000666.1:g.6303098_6303099delinsTT	GRCh37
NC_000004.10:g.6353999_6354000delinsTT	NCBI36
NG_011700.1:g.36522_36523delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1612_1613delinsTT	ENSP00000507852.1:p.Gly538Phe
ENST00000683395.1:c.1553_1554delinsTT
ENST00000684087.1:c.1576_1577delinsTT	ENSP00000506978.1:p.Gly526Phe
ENST00000506362.2:c.1327_1328delinsTT	ENSP00000424103.2:p.Gly443Phe
ENST00000673642.1:c.1235_1236delinsTT	ENSP00000501242.1:p.Gly412Val
ENST00000673991.1:c.1612_1613delinsTT	ENSP00000501033.1:p.Gly538Phe
ENST00000226760.5:c.1576_1577delinsTT MANE Select	ENSP00000226760.1:p.Gly526Phe
ENST00000503569.5:c.1576_1577delinsTT	ENSP00000423337.1:p.Gly526Phe
ENST00000507765.1:n.1761_1762delinsTT
NM_001145853.1:c.1576_1577delinsTT	NP_001139325.1:p.Gly526Phe
NM_006005.3:c.1576_1577delinsTT MANE Select	NP_005996.2:p.Gly526Phe
XM_017008586.1:c.1585_1586delinsTT	XP_016864075.1:p.Gly529Phe