Canonical Allele Identifier: CA1435772135

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301970C= , CM000666.2:g.6301970C=	GRCh38
NC_000004.11:g.6303697C= , CM000666.1:g.6303697C=	GRCh37
NC_000004.10:g.6354598C=	NCBI36
NG_011700.1:g.37121C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2211C=	ENSP00000507852.1:p.Phe737=
ENST00000683395.1:c.2152C=
ENST00000684087.1:c.2175C=	ENSP00000506978.1:p.Phe725=
ENST00000506362.2:c.1926C=	ENSP00000424103.2:p.Phe642=
ENST00000673642.1:c.1834C=	ENSP00000501242.1:n.1834C=
ENST00000673991.1:c.2211C=	ENSP00000501033.1:p.Phe737=
ENST00000226760.5:c.2175C= MANE Select	ENSP00000226760.1:p.Phe725=
ENST00000503569.5:c.2175C=	ENSP00000423337.1:p.Phe725=
ENST00000507765.1:n.2360C=
NM_001145853.1:c.2175C=	NP_001139325.1:p.Phe725=
NM_006005.3:c.2175C= MANE Select	NP_005996.2:p.Phe725=
XM_017008586.1:c.2184C=	XP_016864075.1:p.Phe728=