Canonical Allele Identifier: CA645523667

Gene: WFS1

Linked Data

• COSMIC: COSM1720989

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301076_6301077delinsTT , CM000666.2:g.6301076_6301077delinsTT	GRCh38
NC_000004.11:g.6302803_6302804delinsTT , CM000666.1:g.6302803_6302804delinsTT	GRCh37
NC_000004.10:g.6353704_6353705delinsTT	NCBI36
NG_011700.1:g.36227_36228delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.1317_1318delinsTT	ENSP00000507852.1:p.Pro440Ser
ENST00000683395.1:c.1258_1259delinsTT
ENST00000684087.1:c.1281_1282delinsTT	ENSP00000506978.1:p.Pro428Ser
ENST00000506362.2:c.1032_1033delinsTT	ENSP00000424103.2:p.Pro345Ser
ENST00000673642.1:c.940_941delinsTT	ENSP00000501242.1:p.Pro314Phe
ENST00000673991.1:c.1317_1318delinsTT	ENSP00000501033.1:p.Pro440Ser
ENST00000226760.5:c.1281_1282delinsTT MANE Select	ENSP00000226760.1:p.Pro428Ser
ENST00000503569.5:c.1281_1282delinsTT	ENSP00000423337.1:p.Pro428Ser
ENST00000507765.1:n.1466_1467delinsTT
NM_001145853.1:c.1281_1282delinsTT	NP_001139325.1:p.Pro428Ser
NM_006005.3:c.1281_1282delinsTT MANE Select	NP_005996.2:p.Pro428Ser
XM_017008586.1:c.1290_1291delinsTT	XP_016864075.1:p.Pro431Ser