Canonical Allele Identifier: CA1435772281

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300847A= , CM000666.2:g.6300847A=	GRCh38
NC_000004.11:g.6302574A= , CM000666.1:g.6302574A=	GRCh37
NC_000004.10:g.6353475A=	NCBI36
NG_011700.1:g.35998A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1088A=	ENSP00000507852.1:p.Tyr363=
ENST00000683395.1:c.1029A=
ENST00000684087.1:c.1052A=	ENSP00000506978.1:p.Tyr351=
ENST00000506362.2:c.803A=	ENSP00000424103.2:p.Tyr268=
ENST00000673642.1:c.711A=	ENSP00000501242.1:p.Leu237=
ENST00000673991.1:c.1088A=	ENSP00000501033.1:p.Tyr363=
ENST00000226760.5:c.1052A= MANE Select	ENSP00000226760.1:p.Tyr351=
ENST00000503569.5:c.1052A=	ENSP00000423337.1:p.Tyr351=
ENST00000506362.1:c.685A=
ENST00000507765.1:n.1237A=
NM_001145853.1:c.1052A=	NP_001139325.1:p.Tyr351=
NM_006005.3:c.1052A= MANE Select	NP_005996.2:p.Tyr351=
XM_017008586.1:c.1061A=	XP_016864075.1:p.Tyr354=