Canonical Allele Identifier: CA1435768980

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291978G= , CM000666.2:g.6291978G=	GRCh38
NC_000004.11:g.6293705G= , CM000666.1:g.6293705G=	GRCh37
NC_000004.10:g.6344606G=	NCBI36
NG_011700.1:g.27129G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.693G=	ENSP00000507852.1:p.Glu231=
ENST00000683395.1:c.670G=
ENST00000684087.1:c.693G=	ENSP00000506978.1:p.Glu231=
ENST00000506362.2:c.444G=	ENSP00000424103.2:p.Glu148=
ENST00000673642.1:c.492G=	ENSP00000501242.1:p.Glu164=
ENST00000673991.1:c.693G=	ENSP00000501033.1:p.Glu231=
ENST00000226760.5:c.693G= MANE Select	ENSP00000226760.1:p.Glu231=
ENST00000503569.5:c.693G=	ENSP00000423337.1:p.Glu231=
ENST00000506362.1:c.290G=
ENST00000507765.1:n.878G=
NM_001145853.1:c.693G=	NP_001139325.1:p.Glu231=
NM_006005.3:c.693G= MANE Select	NP_005996.2:p.Glu231=
XM_017008586.1:c.702G=	XP_016864075.1:p.Glu234=