Canonical Allele Identifier: CA1435772259

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300838T= , CM000666.2:g.6300838T=	GRCh38
NC_000004.11:g.6302565T= , CM000666.1:g.6302565T=	GRCh37
NC_000004.10:g.6353466T=	NCBI36
NG_011700.1:g.35989T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1079T=	ENSP00000507852.1:p.Val360=
ENST00000683395.1:c.1020T=
ENST00000684087.1:c.1043T=	ENSP00000506978.1:p.Val348=
ENST00000506362.2:c.794T=	ENSP00000424103.2:p.Val265=
ENST00000673642.1:c.702T=	ENSP00000501242.1:p.Gly234=
ENST00000673991.1:c.1079T=	ENSP00000501033.1:p.Val360=
ENST00000226760.5:c.1043T= MANE Select	ENSP00000226760.1:p.Val348=
ENST00000503569.5:c.1043T=	ENSP00000423337.1:p.Val348=
ENST00000506362.1:c.676T=
ENST00000507765.1:n.1228T=
NM_001145853.1:c.1043T=	NP_001139325.1:p.Val348=
NM_006005.3:c.1043T= MANE Select	NP_005996.2:p.Val348=
XM_017008586.1:c.1052T=	XP_016864075.1:p.Val351=