Canonical Allele Identifier: CA10630747
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 304374
dbSNP Id: rs5030328

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32387926T>A , CM000673.2:g.32387926T>A GRCh38
NC_000011.9:g.32409472T>A , CM000673.1:g.32409472T>A GRCh37
NC_000011.8:g.32366048T>A NCBI36
NG_009272.1:g.52616A>T , LRG_525:g.52616A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.*1132A>T ENSP00000331327.5:n.*1132A>T
ENST00000379077.9:c.*1885A>T ENSP00000368368.5:n.*1885A>T
ENST00000379079.8:c.*1132A>T ENSP00000368370.2:n.*1132A>T
ENST00000452863.10:c.*1132A>T MANE Select ENSP00000415516.5:n.*1132A>T
ENST00000651819.1:n.1626A>T
ENST00000332351.7:c.*1132A>T ENSP00000331327.3:n.*1132A>T
ENST00000379077.7:c.*1885A>T ENSP00000368368.3:n.*1885A>T
ENST00000379079.6:c.*1132A>T ENSP00000368370.2:n.*1132A>T
ENST00000452863.7:c.2626A>T ENSP00000415516.3:n.2626A>T
ENST00000530998.5:c.*1132A>T ENSP00000435307.1:n.*1132A>T
NM_000378.4:c.*1132A>T NP_000369.3:n.*1132A>T
NM_001198551.1:c.*1132A>T , LRG_525t2:c.*1132A>T NP_001185480.1:n.*1132A>T
NM_001198552.1:c.*1132A>T NP_001185481.1:n.*1132A>T
NM_024424.3:c.*1132A>T NP_077742.2:n.*1132A>T
NM_024426.4:c.*1132A>T NP_077744.3:n.*1132A>T
NM_000378.5:c.*1132A>T NP_000369.4:n.*1132A>T
NM_024424.4:c.*1132A>T NP_077742.3:n.*1132A>T
NM_024426.5:c.*1132A>T NP_077744.4:n.*1132A>T
NM_001367854.1:c.*1132A>T NP_001354783.1:n.*1132A>T
NR_160306.1:n.3033A>T
NM_000378.6:c.*1132A>T NP_000369.4:n.*1132A>T
NM_001198552.2:c.*1132A>T NP_001185481.1:n.*1132A>T
NM_024424.5:c.*1132A>T NP_077742.3:n.*1132A>T
NM_024426.6:c.*1132A>T MANE Select NP_077744.4:n.*1132A>T