Canonical Allele Identifier: CA1058888597
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1730449633
gnomAD v3: 4-6291098-T-A
gnomAD v4: 4-6291098-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291098T>A , CM000666.2:g.6291098T>A GRCh38
NC_000004.11:g.6292825T>A , CM000666.1:g.6292825T>A GRCh37
NC_000004.10:g.6343726T>A NCBI36
NG_011700.1:g.26249T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.461-99T>A ENSP00000507852.1:n.461-99T>A
ENST00000683395.1:c.451-99T>A
ENST00000684087.1:c.461-99T>A ENSP00000506978.1:n.461-99T>A
ENST00000684700.1:c.461-99T>A ENSP00000507806.1:n.461-99T>A
ENST00000506362.2:c.212-99T>A ENSP00000424103.2:n.212-99T>A
ENST00000673642.1:c.260-99T>A ENSP00000501242.1:n.260-99T>A
ENST00000673991.1:c.461-99T>A ENSP00000501033.1:n.461-99T>A
ENST00000674051.1:c.335-99T>A ENSP00000501083.1:n.335-99T>A
ENST00000226760.5:c.461-99T>A MANE Select ENSP00000226760.1:n.461-99T>A
ENST00000503569.5:c.461-99T>A ENSP00000423337.1:n.461-99T>A
ENST00000506362.1:c.58-99T>A
ENST00000507765.1:n.646-99T>A
NM_001145853.1:c.461-99T>A NP_001139325.1:n.461-99T>A
NM_006005.3:c.461-99T>A MANE Select NP_005996.2:n.461-99T>A
XM_017008586.1:c.470-99T>A XP_016864075.1:n.470-99T>A