Canonical Allele Identifier: CA1435772848

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302472T= , CM000666.2:g.6302472T=	GRCh38
NC_000004.11:g.6304199T= , CM000666.1:g.6304199T=	GRCh37
NC_000004.10:g.6355100T=	NCBI36
NG_011700.1:g.37623T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*4T=	ENSP00000507852.1:n.*4T=
ENST00000683395.1:c.2654T=
ENST00000684087.1:c.*4T=	ENSP00000506978.1:n.*4T=
ENST00000506362.2:c.*4T=	ENSP00000424103.2:n.*4T=
ENST00000673991.1:c.*4T=	ENSP00000501033.1:n.*4T=
ENST00000226760.5:c.*4T= MANE Select	ENSP00000226760.1:n.*4T=
ENST00000503569.5:c.*4T=	ENSP00000423337.1:n.*4T=
ENST00000507765.1:n.2862T=
NM_001145853.1:c.*4T=	NP_001139325.1:n.*4T=
NM_006005.3:c.*4T= MANE Select	NP_005996.2:n.*4T=
XM_017008586.1:c.*4T=	XP_016864075.1:n.*4T=