Canonical Allele Identifier: CA064680
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32389065G>A , CM000673.2:g.32389065G>A GRCh38
NC_000011.9:g.32410611G>A , CM000673.1:g.32410611G>A GRCh37
NC_000011.8:g.32367187G>A NCBI36
NG_009272.1:g.51477C>T , LRG_525:g.51477C>T

Transcript Alleles

HGVS Amino-acid Change
NM_024426.6:c.1562C>T MANE Select NP_077744.4:p.Ala521Val
ENST00000452863.10:c.1562C>T MANE Select ENSP00000415516.5:p.Ala521Val
NM_000378.4:c.1487C>T NP_000369.3:p.Ala496Val
NM_000378.5:c.1502C>T NP_000369.4:p.Ala501Val
NM_000378.6:c.1502C>T NP_000369.4:p.Ala501Val
NM_001198551.1:c.902C>T , LRG_525t2:c.902C>T NP_001185480.1:p.Ala301Val
NM_001198552.1:c.860C>T NP_001185481.1:p.Ala287Val
NM_001198552.2:c.860C>T NP_001185481.1:p.Ala287Val
NM_001367854.1:c.374C>T NP_001354783.1:p.Ala125Val
NM_024424.3:c.1538C>T NP_077742.2:p.Ala513Val
NM_024424.4:c.1553C>T NP_077742.3:p.Ala518Val
NM_024424.5:c.1553C>T NP_077742.3:p.Ala518Val
NM_024426.4:c.1547C>T NP_077744.3:p.Ala516Val
NM_024426.5:c.1562C>T NP_077744.4:p.Ala521Val
NR_160306.1:n.1894C>T
ENST00000332351.7:c.1547C>T ENSP00000331327.3:p.Ala516Val
ENST00000332351.9:c.1502C>T ENSP00000331327.5:p.Ala501Val
ENST00000379077.7:c.*746C>T ENSP00000368368.3:n.*746C>T
ENST00000379077.9:c.*746C>T ENSP00000368368.5:n.*746C>T
ENST00000379079.6:c.902C>T ENSP00000368370.2:p.Ala301Val
ENST00000379079.8:c.902C>T ENSP00000368370.2:p.Ala301Val
ENST00000448076.7:c.1538C>T ENSP00000413452.3:p.Ala513Val
ENST00000448076.9:c.1553C>T ENSP00000413452.5:p.Ala518Val
ENST00000452863.7:c.1487C>T ENSP00000415516.3:p.Ala496Val
ENST00000527882.5:c.528C>T
ENST00000530998.5:c.860C>T ENSP00000435307.1:p.Ala287Val
ENST00000639563.3:c.1511C>T ENSP00000492269.3:p.Ala504Val
ENST00000639907.2:n.696C>T
ENST00000640146.2:c.887C>T ENSP00000491984.2:p.Ala296Val
ENST00000650745.1:n.1372C>T
ENST00000650861.1:n.2134C>T
ENST00000650986.1:n.225C>T
ENST00000651459.1:c.333C>T
ENST00000651533.1:n.599C>T
ENST00000651668.1:n.499C>T
ENST00000651794.1:n.1405C>T
ENST00000651819.1:n.487C>T
ENST00000652579.1:n.822C>T
ENST00000652724.1:n.752C>T