Canonical Allele Identifier: CA1435773086

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301280C= , CM000666.2:g.6301280C=	GRCh38
NC_000004.11:g.6303007C= , CM000666.1:g.6303007C=	GRCh37
NC_000004.10:g.6353908C=	NCBI36
NG_011700.1:g.36431C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1521C=	ENSP00000507852.1:p.His507=
ENST00000683395.1:c.1462C=
ENST00000684087.1:c.1485C=	ENSP00000506978.1:p.His495=
ENST00000506362.2:c.1236C=	ENSP00000424103.2:p.His412=
ENST00000673642.1:c.1144C=	ENSP00000501242.1:p.Pro382=
ENST00000673991.1:c.1521C=	ENSP00000501033.1:p.His507=
ENST00000226760.5:c.1485C= MANE Select	ENSP00000226760.1:p.His495=
ENST00000503569.5:c.1485C=	ENSP00000423337.1:p.His495=
ENST00000507765.1:n.1670C=
NM_001145853.1:c.1485C=	NP_001139325.1:p.His495=
NM_006005.3:c.1485C= MANE Select	NP_005996.2:p.His495=
XM_017008586.1:c.1494C=	XP_016864075.1:p.His498=