Canonical Allele Identifier: CA549707977

Gene: WFS1

Linked Data

• ClinVar Variation Id: 2801331
• ClinVar RCV Id: RCV003676044
• dbSNP Id: rs1368454663
• gnomAD v2: 4-6293114-G-A
• gnomAD v3: 4-6291387-G-A
• gnomAD v4: 4-6291387-G-A
• MyVariant Identifiers: chr4:g.6293114G>A (hg19) ; chr4:g.6291387G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291387G>A , CM000666.2:g.6291387G>A	GRCh38
NC_000004.11:g.6293114G>A , CM000666.1:g.6293114G>A	GRCh37
NC_000004.10:g.6344015G>A	NCBI36
NG_011700.1:g.26538G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+20G>A	ENSP00000507852.1:n.631+20G>A
ENST00000683395.1:c.608+33G>A
ENST00000684087.1:c.631+20G>A	ENSP00000506978.1:n.631+20G>A
ENST00000684700.1:c.651G>A	ENSP00000507806.1:p.Gly217=
ENST00000506362.2:c.382+20G>A	ENSP00000424103.2:n.382+20G>A
ENST00000673642.1:c.430+20G>A	ENSP00000501242.1:n.430+20G>A
ENST00000673991.1:c.631+20G>A	ENSP00000501033.1:n.631+20G>A
ENST00000226760.5:c.631+20G>A MANE Select	ENSP00000226760.1:n.631+20G>A
ENST00000503569.5:c.631+20G>A	ENSP00000423337.1:n.631+20G>A
ENST00000506362.1:c.228+20G>A
ENST00000507765.1:n.816+20G>A
NM_001145853.1:c.631+20G>A	NP_001139325.1:n.631+20G>A
NM_006005.3:c.631+20G>A MANE Select	NP_005996.2:n.631+20G>A
XM_017008586.1:c.640+20G>A	XP_016864075.1:n.640+20G>A