Canonical Allele Identifier: CA10621491
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 349352
dbSNP Id: rs886059537
gnomAD v4: 4-6302994-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302994A>C , CM000666.2:g.6302994A>C GRCh38
NC_000004.11:g.6304721A>C , CM000666.1:g.6304721A>C GRCh37
NC_000004.10:g.6355622A>C NCBI36
NG_011700.1:g.38145A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*526A>C ENSP00000507852.1:n.*526A>C
ENST00000683395.1:c.3176A>C
ENST00000684087.1:c.*526A>C ENSP00000506978.1:n.*526A>C
ENST00000673991.1:c.*526A>C ENSP00000501033.1:n.*526A>C
ENST00000226760.5:c.*526A>C MANE Select ENSP00000226760.1:n.*526A>C
ENST00000507765.1:n.3384A>C
NM_001145853.1:c.*526A>C NP_001139325.1:n.*526A>C
NM_006005.3:c.*526A>C MANE Select NP_005996.2:n.*526A>C
XM_017008586.1:c.*526A>C XP_016864075.1:n.*526A>C
XR_001741566.2:n.1951T>G