Canonical Allele Identifier: CA1435772858

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301191G= , CM000666.2:g.6301191G=	GRCh38
NC_000004.11:g.6302918G= , CM000666.1:g.6302918G=	GRCh37
NC_000004.10:g.6353819G=	NCBI36
NG_011700.1:g.36342G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1432G=	ENSP00000507852.1:p.Gly478=
ENST00000683395.1:c.1373G=
ENST00000684087.1:c.1396G=	ENSP00000506978.1:p.Gly466=
ENST00000506362.2:c.1147G=	ENSP00000424103.2:p.Gly383=
ENST00000673642.1:c.1055G=	ENSP00000501242.1:p.Arg352=
ENST00000673991.1:c.1432G=	ENSP00000501033.1:p.Gly478=
ENST00000226760.5:c.1396G= MANE Select	ENSP00000226760.1:p.Gly466=
ENST00000503569.5:c.1396G=	ENSP00000423337.1:p.Gly466=
ENST00000507765.1:n.1581G=
NM_001145853.1:c.1396G=	NP_001139325.1:p.Gly466=
NM_006005.3:c.1396G= MANE Select	NP_005996.2:p.Gly466=
XM_017008586.1:c.1405G=	XP_016864075.1:p.Gly469=