Canonical Allele Identifier: CA1962335268
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392015G= , CM000673.2:g.32392015G= GRCh38
NC_000011.9:g.32413561G= , CM000673.1:g.32413561G= GRCh37
NC_000011.8:g.32370137G= NCBI36
NG_009272.1:g.48527C= , LRG_525:g.48527C=

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.1353C= ENSP00000331327.5:p.Ser451=
ENST00000379077.9:c.*588C= ENSP00000368368.5:n.*588C=
ENST00000379079.8:c.753C= ENSP00000368370.2:p.Ser251=
ENST00000448076.9:c.1404C= ENSP00000413452.5:p.Ser468=
ENST00000452863.10:c.1404C= MANE Select ENSP00000415516.5:p.Ser468=
ENST00000526685.2:n.858C=
ENST00000639563.3:c.1353C= ENSP00000492269.3:p.Ser451=
ENST00000639907.2:n.547C=
ENST00000640146.2:c.729C= ENSP00000491984.2:p.Ser243=
ENST00000650745.1:n.1214C=
ENST00000650861.1:n.1985C=
ENST00000650986.1:n.67C=
ENST00000651459.1:c.175C=
ENST00000651533.1:n.450C=
ENST00000651668.1:n.341C=
ENST00000651794.1:n.1247C=
ENST00000651819.1:n.329C=
ENST00000652579.1:n.664C=
ENST00000652724.1:n.594C=
ENST00000332351.7:c.1389C= ENSP00000331327.3:p.Ser463=
ENST00000379077.7:c.*588C= ENSP00000368368.3:n.*588C=
ENST00000379079.6:c.753C= ENSP00000368370.2:p.Ser251=
ENST00000448076.7:c.1389C= ENSP00000413452.3:p.Ser463=
ENST00000452863.7:c.1338C= ENSP00000415516.3:p.Ser446=
ENST00000527882.5:c.370C=
ENST00000530998.5:c.702C= ENSP00000435307.1:p.Ser234=
NM_000378.4:c.1338C= NP_000369.3:p.Ser446=
NM_001198551.1:c.753C= , LRG_525t2:c.753C= NP_001185480.1:p.Ser251=
NM_001198552.1:c.702C= NP_001185481.1:p.Ser234=
NM_024424.3:c.1389C= NP_077742.2:p.Ser463=
NM_024426.4:c.1389C= NP_077744.3:p.Ser463=
NM_000378.5:c.1353C= NP_000369.4:p.Ser451=
NM_024424.4:c.1404C= NP_077742.3:p.Ser468=
NM_024426.5:c.1404C= NP_077744.4:p.Ser468=
NM_001367854.1:c.216C= NP_001354783.1:p.Ser72=
NR_160306.1:n.1736C=
NM_000378.6:c.1353C= NP_000369.4:p.Ser451=
NM_001198552.2:c.702C= NP_001185481.1:p.Ser234=
NM_024424.5:c.1404C= NP_077742.3:p.Ser468=
NM_024426.6:c.1404C= MANE Select NP_077744.4:p.Ser468=