Canonical Allele Identifier: CA2669843060

Gene: WFS1

Linked Data

• gnomAD v4: 4-6300529-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300529C>G , CM000666.2:g.6300529C>G	GRCh38
NC_000004.11:g.6302256C>G , CM000666.1:g.6302256C>G	GRCh37
NC_000004.10:g.6353157C>G	NCBI36
NG_011700.1:g.35680C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-128C>G	ENSP00000507852.1:n.898-128C>G
ENST00000683395.1:c.839-128C>G
ENST00000684087.1:c.862-128C>G	ENSP00000506978.1:n.862-128C>G
ENST00000506362.2:c.613-128C>G	ENSP00000424103.2:n.613-128C>G
ENST00000673642.1:c.661-268C>G	ENSP00000501242.1:n.661-268C>G
ENST00000673991.1:c.898-128C>G	ENSP00000501033.1:n.898-128C>G
ENST00000226760.5:c.862-128C>G MANE Select	ENSP00000226760.1:n.862-128C>G
ENST00000503569.5:c.862-128C>G	ENSP00000423337.1:n.862-128C>G
ENST00000506362.1:c.495-128C>G
ENST00000507765.1:n.1047-128C>G
ENST00000513395.1:n.420-128C>G
NM_001145853.1:c.862-128C>G	NP_001139325.1:n.862-128C>G
NM_006005.3:c.862-128C>G MANE Select	NP_005996.2:n.862-128C>G
XM_017008586.1:c.871-128C>G	XP_016864075.1:n.871-128C>G