Canonical Allele Identifier: CA438210938

Gene: WFS1

Linked Data

• gnomAD v4: 4-6291222-G-A
• MyVariant Identifiers: chr4:g.6292949G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291222G>A , CM000666.2:g.6291222G>A	GRCh38
NC_000004.11:g.6292949G>A , CM000666.1:g.6292949G>A	GRCh37
NC_000004.10:g.6343850G>A	NCBI36
NG_011700.1:g.26373G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.486G>A	ENSP00000507852.1:p.Glu162=
ENST00000683395.1:c.476G>A
ENST00000684087.1:c.486G>A	ENSP00000506978.1:p.Glu162=
ENST00000684700.1:c.486G>A	ENSP00000507806.1:p.Glu162=
ENST00000506362.2:c.237G>A	ENSP00000424103.2:p.Glu79=
ENST00000673642.1:c.285G>A	ENSP00000501242.1:p.Glu95=
ENST00000673991.1:c.486G>A	ENSP00000501033.1:p.Glu162=
ENST00000674051.1:c.360G>A	ENSP00000501083.1:p.Glu120=
ENST00000226760.5:c.486G>A MANE Select	ENSP00000226760.1:p.Glu162=
ENST00000503569.5:c.486G>A	ENSP00000423337.1:p.Glu162=
ENST00000506362.1:c.83G>A
ENST00000507765.1:n.671G>A
NM_001145853.1:c.486G>A	NP_001139325.1:p.Glu162=
NM_006005.3:c.486G>A MANE Select	NP_005996.2:p.Glu162=
XM_017008586.1:c.495G>A	XP_016864075.1:p.Glu165=