Canonical Allele Identifier: CA2669843439

Gene: WFS1

Linked Data

• gnomAD v4: 4-6301294-A-ATGT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301294_6301295insTGT , CM000666.2:g.6301294_6301295insTGT	GRCh38
NC_000004.11:g.6303021_6303022insTGT , CM000666.1:g.6303021_6303022insTGT	GRCh37
NC_000004.10:g.6353922_6353923insTGT	NCBI36
NG_011700.1:g.36445_36446insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1535_1536insTGT	ENSP00000507852.1:p.Asn512_Val513insVal
ENST00000683395.1:c.1476_1477insTGT
ENST00000684087.1:c.1499_1500insTGT	ENSP00000506978.1:p.Asn500_Val501insVal
ENST00000506362.2:c.1250_1251insTGT	ENSP00000424103.2:p.Asn417_Val418insVal
ENST00000673642.1:c.1158_1159insTGT	ENSP00000501242.1:p.Gln386_Arg387insCys
ENST00000673991.1:c.1535_1536insTGT	ENSP00000501033.1:p.Asn512_Val513insVal
ENST00000226760.5:c.1499_1500insTGT MANE Select	ENSP00000226760.1:p.Asn500_Val501insVal
ENST00000503569.5:c.1499_1500insTGT	ENSP00000423337.1:p.Asn500_Val501insVal
ENST00000507765.1:n.1684_1685insTGT
NM_001145853.1:c.1499_1500insTGT	NP_001139325.1:p.Asn500_Val501insVal
NM_006005.3:c.1499_1500insTGT MANE Select	NP_005996.2:p.Asn500_Val501insVal
XM_017008586.1:c.1508_1509insTGT	XP_016864075.1:p.Asn503_Val504insVal