Canonical Allele Identifier: CA1435774014

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301563A= , CM000666.2:g.6301563A=	GRCh38
NC_000004.11:g.6303290A= , CM000666.1:g.6303290A=	GRCh37
NC_000004.10:g.6354191A=	NCBI36
NG_011700.1:g.36714A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1804A=	ENSP00000507852.1:p.Thr602=
ENST00000683395.1:c.1745A=
ENST00000684087.1:c.1768A=	ENSP00000506978.1:p.Thr590=
ENST00000506362.2:c.1519A=	ENSP00000424103.2:p.Thr507=
ENST00000673642.1:c.1427A=	ENSP00000501242.1:n.1427A=
ENST00000673991.1:c.1804A=	ENSP00000501033.1:p.Thr602=
ENST00000226760.5:c.1768A= MANE Select	ENSP00000226760.1:p.Thr590=
ENST00000503569.5:c.1768A=	ENSP00000423337.1:p.Thr590=
ENST00000507765.1:n.1953A=
NM_001145853.1:c.1768A=	NP_001139325.1:p.Thr590=
NM_006005.3:c.1768A= MANE Select	NP_005996.2:p.Thr590=
XM_017008586.1:c.1777A=	XP_016864075.1:p.Thr593=