Canonical Allele Identifier: CA1435771996

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300688A= , CM000666.2:g.6300688A=	GRCh38
NC_000004.11:g.6302415A= , CM000666.1:g.6302415A=	GRCh37
NC_000004.10:g.6353316A=	NCBI36
NG_011700.1:g.35839A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.929A=	ENSP00000507852.1:p.Glu310=
ENST00000683395.1:c.870A=
ENST00000684087.1:c.893A=	ENSP00000506978.1:p.Glu298=
ENST00000506362.2:c.644A=	ENSP00000424103.2:p.Glu215=
ENST00000673642.1:c.661-109A=	ENSP00000501242.1:n.661-109A=
ENST00000673991.1:c.929A=	ENSP00000501033.1:p.Glu310=
ENST00000226760.5:c.893A= MANE Select	ENSP00000226760.1:p.Glu298=
ENST00000503569.5:c.893A=	ENSP00000423337.1:p.Glu298=
ENST00000506362.1:c.526A=
ENST00000507765.1:n.1078A=
ENST00000513395.1:n.451A=
NM_001145853.1:c.893A=	NP_001139325.1:p.Glu298=
NM_006005.3:c.893A= MANE Select	NP_005996.2:p.Glu298=
XM_017008586.1:c.902A=	XP_016864075.1:p.Glu301=