Canonical Allele Identifier: CA2669843660

Gene: WFS1

Linked Data

• dbSNP Id: rs2109128306
• gnomAD v4: 4-6302635-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302635A>G , CM000666.2:g.6302635A>G	GRCh38
NC_000004.11:g.6304362A>G , CM000666.1:g.6304362A>G	GRCh37
NC_000004.10:g.6355263A>G	NCBI36
NG_011700.1:g.37786A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*167A>G	ENSP00000507852.1:n.*167A>G
ENST00000683395.1:c.2817A>G
ENST00000684087.1:c.*167A>G	ENSP00000506978.1:n.*167A>G
ENST00000506362.2:c.*167A>G	ENSP00000424103.2:n.*167A>G
ENST00000673991.1:c.*167A>G	ENSP00000501033.1:n.*167A>G
ENST00000226760.5:c.*167A>G MANE Select	ENSP00000226760.1:n.*167A>G
ENST00000503569.5:c.*167A>G	ENSP00000423337.1:n.*167A>G
ENST00000507765.1:n.3025A>G
NM_001145853.1:c.*167A>G	NP_001139325.1:n.*167A>G
NM_006005.3:c.*167A>G MANE Select	NP_005996.2:n.*167A>G
XM_017008586.1:c.*167A>G	XP_016864075.1:n.*167A>G