Canonical Allele Identifier: CA2839762
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs762556590
gnomAD v2: 4-6304043-G-T
gnomAD v4: 4-6302316-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302316G>T , CM000666.2:g.6302316G>T GRCh38
NC_000004.11:g.6304043G>T , CM000666.1:g.6304043G>T GRCh37
NC_000004.10:g.6354944G>T NCBI36
NG_011700.1:g.37467G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2557G>T ENSP00000507852.1:p.Glu853Ter
ENST00000683395.1:c.2498G>T
ENST00000684087.1:c.2521G>T ENSP00000506978.1:p.Glu841Ter
ENST00000506362.2:c.2272G>T ENSP00000424103.2:p.Glu758Ter
ENST00000673991.1:c.2557G>T ENSP00000501033.1:p.Glu853Ter
ENST00000226760.5:c.2521G>T MANE Select ENSP00000226760.1:p.Glu841Ter
ENST00000503569.5:c.2521G>T ENSP00000423337.1:p.Glu841Ter
ENST00000507765.1:n.2706G>T
NM_001145853.1:c.2521G>T NP_001139325.1:p.Glu841Ter
NM_006005.3:c.2521G>T MANE Select NP_005996.2:p.Glu841Ter
XM_017008586.1:c.2530G>T XP_016864075.1:p.Glu844Ter