Canonical Allele Identifier: CA1435771995

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301870A= , CM000666.2:g.6301870A=	GRCh38
NC_000004.11:g.6303597A= , CM000666.1:g.6303597A=	GRCh37
NC_000004.10:g.6354498A=	NCBI36
NG_011700.1:g.37021A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2111A=	ENSP00000507852.1:p.His704=
ENST00000683395.1:c.2052A=
ENST00000684087.1:c.2075A=	ENSP00000506978.1:p.His692=
ENST00000506362.2:c.1826A=	ENSP00000424103.2:p.His609=
ENST00000673642.1:c.1734A=	ENSP00000501242.1:n.1734A=
ENST00000673991.1:c.2111A=	ENSP00000501033.1:p.His704=
ENST00000226760.5:c.2075A= MANE Select	ENSP00000226760.1:p.His692=
ENST00000503569.5:c.2075A=	ENSP00000423337.1:p.His692=
ENST00000507765.1:n.2260A=
NM_001145853.1:c.2075A=	NP_001139325.1:p.His692=
NM_006005.3:c.2075A= MANE Select	NP_005996.2:p.His692=
XM_017008586.1:c.2084A=	XP_016864075.1:p.His695=