Canonical Allele Identifier: CA1435773496

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6303068T= , CM000666.2:g.6303068T=	GRCh38
NC_000004.11:g.6304795T= , CM000666.1:g.6304795T=	GRCh37
NC_000004.10:g.6355696T=	NCBI36
NG_011700.1:g.38219T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*600T=	ENSP00000507852.1:n.*600T=
ENST00000683395.1:c.3250T=
ENST00000684087.1:c.*600T=	ENSP00000506978.1:n.*600T=
ENST00000673991.1:c.*600T=	ENSP00000501033.1:n.*600T=
ENST00000226760.5:c.*600T= MANE Select	ENSP00000226760.1:n.*600T=
ENST00000507765.1:n.3458T=
NM_001145853.1:c.*600T=	NP_001139325.1:n.*600T=
NM_006005.3:c.*600T= MANE Select	NP_005996.2:n.*600T=
XM_017008586.1:c.*600T=	XP_016864075.1:n.*600T=
XR_001741566.2:n.1877A=