Canonical Allele Identifier: CA1435772456

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302190A= , CM000666.2:g.6302190A=	GRCh38
NC_000004.11:g.6303917A= , CM000666.1:g.6303917A=	GRCh37
NC_000004.10:g.6354818A=	NCBI36
NG_011700.1:g.37341A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.2431A=	ENSP00000507852.1:p.Thr811=
ENST00000683395.1:c.2372A=
ENST00000684087.1:c.2395A=	ENSP00000506978.1:p.Thr799=
ENST00000506362.2:c.2146A=	ENSP00000424103.2:p.Thr716=
ENST00000673991.1:c.2431A=	ENSP00000501033.1:p.Thr811=
ENST00000226760.5:c.2395A= MANE Select	ENSP00000226760.1:p.Thr799=
ENST00000503569.5:c.2395A=	ENSP00000423337.1:p.Thr799=
ENST00000507765.1:n.2580A=
NM_001145853.1:c.2395A=	NP_001139325.1:p.Thr799=
NM_006005.3:c.2395A= MANE Select	NP_005996.2:p.Thr799=
XM_017008586.1:c.2404A=	XP_016864075.1:p.Thr802=