Canonical Allele Identifier: CA1435772332

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302104T= , CM000666.2:g.6302104T=	GRCh38
NC_000004.11:g.6303831T= , CM000666.1:g.6303831T=	GRCh37
NC_000004.10:g.6354732T=	NCBI36
NG_011700.1:g.37255T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.2345T=	ENSP00000507852.1:p.Phe782=
ENST00000683395.1:c.2286T=
ENST00000684087.1:c.2309T=	ENSP00000506978.1:p.Phe770=
ENST00000506362.2:c.2060T=	ENSP00000424103.2:p.Phe687=
ENST00000673642.1:c.1968T=	ENSP00000501242.1:n.1968T=
ENST00000673991.1:c.2345T=	ENSP00000501033.1:p.Phe782=
ENST00000226760.5:c.2309T= MANE Select	ENSP00000226760.1:p.Phe770=
ENST00000503569.5:c.2309T=	ENSP00000423337.1:p.Phe770=
ENST00000507765.1:n.2494T=
NM_001145853.1:c.2309T=	NP_001139325.1:p.Phe770=
NM_006005.3:c.2309T= MANE Select	NP_005996.2:p.Phe770=
XM_017008586.1:c.2318T=	XP_016864075.1:p.Phe773=