Canonical Allele Identifier: CA1435771979

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301854C= , CM000666.2:g.6301854C=	GRCh38
NC_000004.11:g.6303581C= , CM000666.1:g.6303581C=	GRCh37
NC_000004.10:g.6354482C=	NCBI36
NG_011700.1:g.37005C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2095C=	ENSP00000507852.1:p.Gln699=
ENST00000683395.1:c.2036C=
ENST00000684087.1:c.2059C=	ENSP00000506978.1:p.Gln687=
ENST00000506362.2:c.1810C=	ENSP00000424103.2:p.Gln604=
ENST00000673642.1:c.1718C=	ENSP00000501242.1:n.1718C=
ENST00000673991.1:c.2095C=	ENSP00000501033.1:p.Gln699=
ENST00000226760.5:c.2059C= MANE Select	ENSP00000226760.1:p.Gln687=
ENST00000503569.5:c.2059C=	ENSP00000423337.1:p.Gln687=
ENST00000507765.1:n.2244C=
NM_001145853.1:c.2059C=	NP_001139325.1:p.Gln687=
NM_006005.3:c.2059C= MANE Select	NP_005996.2:p.Gln687=
XM_017008586.1:c.2068C=	XP_016864075.1:p.Gln690=