Canonical Allele Identifier: CA1435772302

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300859T= , CM000666.2:g.6300859T=	GRCh38
NC_000004.11:g.6302586T= , CM000666.1:g.6302586T=	GRCh37
NC_000004.10:g.6353487T=	NCBI36
NG_011700.1:g.36010T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1100T=	ENSP00000507852.1:p.Ile367=
ENST00000683395.1:c.1041T=
ENST00000684087.1:c.1064T=	ENSP00000506978.1:p.Ile355=
ENST00000506362.2:c.815T=	ENSP00000424103.2:p.Ile272=
ENST00000673642.1:c.723T=	ENSP00000501242.1:p.His241=
ENST00000673991.1:c.1100T=	ENSP00000501033.1:p.Ile367=
ENST00000226760.5:c.1064T= MANE Select	ENSP00000226760.1:p.Ile355=
ENST00000503569.5:c.1064T=	ENSP00000423337.1:p.Ile355=
ENST00000506362.1:c.697T=
ENST00000507765.1:n.1249T=
NM_001145853.1:c.1064T=	NP_001139325.1:p.Ile355=
NM_006005.3:c.1064T= MANE Select	NP_005996.2:p.Ile355=
XM_017008586.1:c.1073T=	XP_016864075.1:p.Ile358=