Canonical Allele Identifier: CA1435774115

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301591T= , CM000666.2:g.6301591T=	GRCh38
NC_000004.11:g.6303318T= , CM000666.1:g.6303318T=	GRCh37
NC_000004.10:g.6354219T=	NCBI36
NG_011700.1:g.36742T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1832T=	ENSP00000507852.1:p.Val611=
ENST00000683395.1:c.1773T=
ENST00000684087.1:c.1796T=	ENSP00000506978.1:p.Val599=
ENST00000506362.2:c.1547T=	ENSP00000424103.2:p.Val516=
ENST00000673642.1:c.1455T=	ENSP00000501242.1:n.1455T=
ENST00000673991.1:c.1832T=	ENSP00000501033.1:p.Val611=
ENST00000226760.5:c.1796T= MANE Select	ENSP00000226760.1:p.Val599=
ENST00000503569.5:c.1796T=	ENSP00000423337.1:p.Val599=
ENST00000507765.1:n.1981T=
NM_001145853.1:c.1796T=	NP_001139325.1:p.Val599=
NM_006005.3:c.1796T= MANE Select	NP_005996.2:p.Val599=
XM_017008586.1:c.1805T=	XP_016864075.1:p.Val602=