Canonical Allele Identifier: CA1435768957

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291941T= , CM000666.2:g.6291941T=	GRCh38
NC_000004.11:g.6293668T= , CM000666.1:g.6293668T=	GRCh37
NC_000004.10:g.6344569T=	NCBI36
NG_011700.1:g.27092T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.656T=	ENSP00000507852.1:p.Val219=
ENST00000683395.1:c.633T=
ENST00000684087.1:c.656T=	ENSP00000506978.1:p.Val219=
ENST00000506362.2:c.407T=	ENSP00000424103.2:p.Val136=
ENST00000673642.1:c.455T=	ENSP00000501242.1:p.Val152=
ENST00000673991.1:c.656T=	ENSP00000501033.1:p.Val219=
ENST00000226760.5:c.656T= MANE Select	ENSP00000226760.1:p.Val219=
ENST00000503569.5:c.656T=	ENSP00000423337.1:p.Val219=
ENST00000506362.1:c.253T=
ENST00000507765.1:n.841T=
NM_001145853.1:c.656T=	NP_001139325.1:p.Val219=
NM_006005.3:c.656T= MANE Select	NP_005996.2:p.Val219=
XM_017008586.1:c.665T=	XP_016864075.1:p.Val222=