Canonical Allele Identifier: CA1435768629

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291331G= , CM000666.2:g.6291331G=	GRCh38
NC_000004.11:g.6293058G= , CM000666.1:g.6293058G=	GRCh37
NC_000004.10:g.6343959G=	NCBI36
NG_011700.1:g.26482G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.595G=	ENSP00000507852.1:p.Glu199=
ENST00000683395.1:c.585G=
ENST00000684087.1:c.595G=	ENSP00000506978.1:p.Glu199=
ENST00000684700.1:c.595G=	ENSP00000507806.1:p.Glu199=
ENST00000506362.2:c.346G=	ENSP00000424103.2:p.Glu116=
ENST00000673642.1:c.394G=	ENSP00000501242.1:p.Glu132=
ENST00000673991.1:c.595G=	ENSP00000501033.1:p.Glu199=
ENST00000226760.5:c.595G= MANE Select	ENSP00000226760.1:p.Glu199=
ENST00000503569.5:c.595G=	ENSP00000423337.1:p.Glu199=
ENST00000506362.1:c.192G=
ENST00000507765.1:n.780G=
NM_001145853.1:c.595G=	NP_001139325.1:p.Glu199=
NM_006005.3:c.595G= MANE Select	NP_005996.2:p.Glu199=
XM_017008586.1:c.604G=	XP_016864075.1:p.Glu202=