Canonical Allele Identifier: CA10638319
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 304406
dbSNP Id: rs886048223

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32388692G>T , CM000673.2:g.32388692G>T GRCh38
NC_000011.9:g.32410238G>T , CM000673.1:g.32410238G>T GRCh37
NC_000011.8:g.32366814G>T NCBI36
NG_009272.1:g.51850C>A , LRG_525:g.51850C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.*366C>A ENSP00000331327.5:n.*366C>A
ENST00000379077.9:c.*1119C>A ENSP00000368368.5:n.*1119C>A
ENST00000379079.8:c.*366C>A ENSP00000368370.2:n.*366C>A
ENST00000448076.9:c.*366C>A ENSP00000413452.5:n.*366C>A
ENST00000452863.10:c.*366C>A MANE Select ENSP00000415516.5:n.*366C>A
ENST00000639907.2:n.1069C>A
ENST00000640146.2:c.*366C>A ENSP00000491984.2:n.*366C>A
ENST00000650745.1:n.1745C>A
ENST00000650861.1:n.2507C>A
ENST00000651459.1:c.706C>A
ENST00000651533.1:n.972C>A
ENST00000651668.1:n.872C>A
ENST00000651794.1:n.1778C>A
ENST00000651819.1:n.860C>A
ENST00000652579.1:n.1195C>A
ENST00000652724.1:n.1125C>A
ENST00000332351.7:c.*366C>A ENSP00000331327.3:n.*366C>A
ENST00000379077.7:c.*1119C>A ENSP00000368368.3:n.*1119C>A
ENST00000379079.6:c.*366C>A ENSP00000368370.2:n.*366C>A
ENST00000448076.7:c.*366C>A ENSP00000413452.3:n.*366C>A
ENST00000452863.7:c.1860C>A ENSP00000415516.3:n.1860C>A
ENST00000530998.5:c.*366C>A ENSP00000435307.1:n.*366C>A
NM_000378.4:c.*366C>A NP_000369.3:n.*366C>A
NM_001198551.1:c.*366C>A , LRG_525t2:c.*366C>A NP_001185480.1:n.*366C>A
NM_001198552.1:c.*366C>A NP_001185481.1:n.*366C>A
NM_024424.3:c.*366C>A NP_077742.2:n.*366C>A
NM_024426.4:c.*366C>A NP_077744.3:n.*366C>A
NM_000378.5:c.*366C>A NP_000369.4:n.*366C>A
NM_024424.4:c.*366C>A NP_077742.3:n.*366C>A
NM_024426.5:c.*366C>A NP_077744.4:n.*366C>A
NM_001367854.1:c.*366C>A NP_001354783.1:n.*366C>A
NR_160306.1:n.2267C>A
NM_000378.6:c.*366C>A NP_000369.4:n.*366C>A
NM_001198552.2:c.*366C>A NP_001185481.1:n.*366C>A
NM_024424.5:c.*366C>A NP_077742.3:n.*366C>A
NM_024426.6:c.*366C>A MANE Select NP_077744.4:n.*366C>A