Canonical Allele Identifier: CA356171906

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6292960T>A (hg19) ; chr4:g.6291233T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291233T>A , CM000666.2:g.6291233T>A	GRCh38
NC_000004.11:g.6292960T>A , CM000666.1:g.6292960T>A	GRCh37
NC_000004.10:g.6343861T>A	NCBI36
NG_011700.1:g.26384T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.497T>A	ENSP00000507852.1:p.Leu166His
ENST00000683395.1:c.487T>A
ENST00000684087.1:c.497T>A	ENSP00000506978.1:p.Leu166His
ENST00000684700.1:c.497T>A	ENSP00000507806.1:p.Leu166His
ENST00000506362.2:c.248T>A	ENSP00000424103.2:p.Leu83His
ENST00000673642.1:c.296T>A	ENSP00000501242.1:p.Leu99His
ENST00000673991.1:c.497T>A	ENSP00000501033.1:p.Leu166His
ENST00000674051.1:c.371T>A	ENSP00000501083.1:p.Leu124His
ENST00000226760.5:c.497T>A MANE Select	ENSP00000226760.1:p.Leu166His
ENST00000503569.5:c.497T>A	ENSP00000423337.1:p.Leu166His
ENST00000506362.1:c.94T>A
ENST00000507765.1:n.682T>A
NM_001145853.1:c.497T>A	NP_001139325.1:p.Leu166His
NM_006005.3:c.497T>A MANE Select	NP_005996.2:p.Leu166His
XM_017008586.1:c.506T>A	XP_016864075.1:p.Leu169His