Canonical Allele Identifier: CA1435773248

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301325C= , CM000666.2:g.6301325C=	GRCh38
NC_000004.11:g.6303052C= , CM000666.1:g.6303052C=	GRCh37
NC_000004.10:g.6353953C=	NCBI36
NG_011700.1:g.36476C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1566C=	ENSP00000507852.1:p.Tyr522=
ENST00000683395.1:c.1507C=
ENST00000684087.1:c.1530C=	ENSP00000506978.1:p.Tyr510=
ENST00000506362.2:c.1281C=	ENSP00000424103.2:p.Tyr427=
ENST00000673642.1:c.1189C=	ENSP00000501242.1:p.Pro397=
ENST00000673991.1:c.1566C=	ENSP00000501033.1:p.Tyr522=
ENST00000226760.5:c.1530C= MANE Select	ENSP00000226760.1:p.Tyr510=
ENST00000503569.5:c.1530C=	ENSP00000423337.1:p.Tyr510=
ENST00000507765.1:n.1715C=
NM_001145853.1:c.1530C=	NP_001139325.1:p.Tyr510=
NM_006005.3:c.1530C= MANE Select	NP_005996.2:p.Tyr510=
XM_017008586.1:c.1539C=	XP_016864075.1:p.Tyr513=