Canonical Allele Identifier: CA2839360
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1417343
ClinVar RCV Id: RCV001938300
dbSNP Id: rs142269405
gnomAD v2: 4-6302982-C-G
gnomAD v3: 4-6301255-C-G
gnomAD v4: 4-6301255-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301255C>G , CM000666.2:g.6301255C>G GRCh38
NC_000004.11:g.6302982C>G , CM000666.1:g.6302982C>G GRCh37
NC_000004.10:g.6353883C>G NCBI36
NG_011700.1:g.36406C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.1496C>G ENSP00000507852.1:p.Thr499Ser
ENST00000683395.1:c.1437C>G
ENST00000684087.1:c.1460C>G ENSP00000506978.1:p.Thr487Ser
ENST00000506362.2:c.1211C>G ENSP00000424103.2:p.Thr404Ser
ENST00000673642.1:c.1119C>G ENSP00000501242.1:p.Asp373Glu
ENST00000673991.1:c.1496C>G ENSP00000501033.1:p.Thr499Ser
ENST00000226760.5:c.1460C>G MANE Select ENSP00000226760.1:p.Thr487Ser
ENST00000503569.5:c.1460C>G ENSP00000423337.1:p.Thr487Ser
ENST00000507765.1:n.1645C>G
NM_001145853.1:c.1460C>G NP_001139325.1:p.Thr487Ser
NM_006005.3:c.1460C>G MANE Select NP_005996.2:p.Thr487Ser
XM_017008586.1:c.1469C>G XP_016864075.1:p.Thr490Ser