Canonical Allele Identifier: CA1435773734

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301487C= , CM000666.2:g.6301487C=	GRCh38
NC_000004.11:g.6303214C= , CM000666.1:g.6303214C=	GRCh37
NC_000004.10:g.6354115C=	NCBI36
NG_011700.1:g.36638C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1728C=	ENSP00000507852.1:p.Phe576=
ENST00000683395.1:c.1669C=
ENST00000684087.1:c.1692C=	ENSP00000506978.1:p.Phe564=
ENST00000506362.2:c.1443C=	ENSP00000424103.2:p.Phe481=
ENST00000673642.1:c.1351C=	ENSP00000501242.1:n.1351C=
ENST00000673991.1:c.1728C=	ENSP00000501033.1:p.Phe576=
ENST00000226760.5:c.1692C= MANE Select	ENSP00000226760.1:p.Phe564=
ENST00000503569.5:c.1692C=	ENSP00000423337.1:p.Phe564=
ENST00000507765.1:n.1877C=
NM_001145853.1:c.1692C=	NP_001139325.1:p.Phe564=
NM_006005.3:c.1692C= MANE Select	NP_005996.2:p.Phe564=
XM_017008586.1:c.1701C=	XP_016864075.1:p.Phe567=