Canonical Allele Identifier: CA356173797
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1402207631
gnomAD v3: 4-6300670-C-A
gnomAD v4: 4-6300670-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6300670C>A , CM000666.2:g.6300670C>A GRCh38
NC_000004.11:g.6302397C>A , CM000666.1:g.6302397C>A GRCh37
NC_000004.10:g.6353298C>A NCBI36
NG_011700.1:g.35821C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.911C>A ENSP00000507852.1:p.Pro304His
ENST00000683395.1:c.852C>A
ENST00000684087.1:c.875C>A ENSP00000506978.1:p.Pro292His
ENST00000506362.2:c.626C>A ENSP00000424103.2:p.Pro209His
ENST00000673642.1:c.661-127C>A ENSP00000501242.1:n.661-127C>A
ENST00000673991.1:c.911C>A ENSP00000501033.1:p.Pro304His
ENST00000226760.5:c.875C>A MANE Select ENSP00000226760.1:p.Pro292His
ENST00000503569.5:c.875C>A ENSP00000423337.1:p.Pro292His
ENST00000506362.1:c.508C>A
ENST00000507765.1:n.1060C>A
ENST00000513395.1:n.433C>A
NM_001145853.1:c.875C>A NP_001139325.1:p.Pro292His
NM_006005.3:c.875C>A MANE Select NP_005996.2:p.Pro292His
XM_017008586.1:c.884C>A XP_016864075.1:p.Pro295His