Canonical Allele Identifier: CA1962337984
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32396313C= , CM000673.2:g.32396313C= GRCh38
NC_000011.9:g.32417859C= , CM000673.1:g.32417859C= GRCh37
NC_000011.8:g.32374435C= NCBI36
NG_009272.1:g.44229G= , LRG_525:g.44229G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1157G= ENSP00000331327.5:p.Cys386=
ENST00000379077.9:c.*392G= ENSP00000368368.5:n.*392G=
ENST00000379079.8:c.557G= ENSP00000368370.2:p.Cys186=
ENST00000448076.9:c.1208G= ENSP00000413452.5:p.Cys403=
ENST00000452863.10:c.1208G= MANE Select ENSP00000415516.5:p.Cys403=
ENST00000526685.2:n.662G=
ENST00000639563.3:c.1157G= ENSP00000492269.3:p.Cys386=
ENST00000639907.2:n.351G=
ENST00000640146.2:c.533G= ENSP00000491984.2:p.Cys178=
ENST00000650861.1:n.1789G=
ENST00000651459.1:c.36-3558G=
ENST00000651668.1:n.145G=
ENST00000651794.1:n.951G=
ENST00000651819.1:n.133G=
ENST00000652579.1:n.368G=
ENST00000652724.1:n.398G=
ENST00000332351.7:c.1193G= ENSP00000331327.3:p.Cys398=
ENST00000379077.7:c.*392G= ENSP00000368368.3:n.*392G=
ENST00000379079.6:c.557G= ENSP00000368370.2:p.Cys186=
ENST00000448076.7:c.1193G= ENSP00000413452.3:p.Cys398=
ENST00000452863.7:c.1142G= ENSP00000415516.3:p.Cys381=
ENST00000526685.1:c.20G= ENSP00000436292.1:p.Cys7=
ENST00000527882.5:c.264G=
ENST00000530998.5:c.506G= ENSP00000435307.1:p.Cys169=
NM_000378.4:c.1142G= NP_000369.3:p.Cys381=
NM_001198551.1:c.557G= , LRG_525t2:c.557G= NP_001185480.1:p.Cys186=
NM_001198552.1:c.506G= NP_001185481.1:p.Cys169=
NM_024424.3:c.1193G= NP_077742.2:p.Cys398=
NM_024426.4:c.1193G= NP_077744.3:p.Cys398=
NM_000378.5:c.1157G= NP_000369.4:p.Cys386=
NM_024424.4:c.1208G= NP_077742.3:p.Cys403=
NM_024426.5:c.1208G= NP_077744.4:p.Cys403=
NM_001367854.1:c.20G= NP_001354783.1:p.Cys7=
NR_160306.1:n.1540G=
NM_000378.6:c.1157G= NP_000369.4:p.Cys386=
NM_001198552.2:c.506G= NP_001185481.1:p.Cys169=
NM_024424.5:c.1208G= NP_077742.3:p.Cys403=
NM_024426.6:c.1208G= MANE Select NP_077744.4:p.Cys403=