Canonical Allele Identifier: CA1962335275
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392026A= , CM000673.2:g.32392026A= GRCh38
NC_000011.9:g.32413572A= , CM000673.1:g.32413572A= GRCh37
NC_000011.8:g.32370148A= NCBI36
NG_009272.1:g.48516T= , LRG_525:g.48516T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1342T= ENSP00000331327.5:p.Phe448=
ENST00000379077.9:c.*577T= ENSP00000368368.5:n.*577T=
ENST00000379079.8:c.742T= ENSP00000368370.2:p.Phe248=
ENST00000448076.9:c.1393T= ENSP00000413452.5:p.Phe465=
ENST00000452863.10:c.1393T= MANE Select ENSP00000415516.5:p.Phe465=
ENST00000526685.2:n.847T=
ENST00000639563.3:c.1342T= ENSP00000492269.3:p.Phe448=
ENST00000639907.2:n.536T=
ENST00000640146.2:c.718T= ENSP00000491984.2:p.Phe240=
ENST00000650745.1:n.1203T=
ENST00000650861.1:n.1974T=
ENST00000650986.1:n.56T=
ENST00000651459.1:c.164T=
ENST00000651533.1:n.439T=
ENST00000651668.1:n.330T=
ENST00000651794.1:n.1236T=
ENST00000651819.1:n.318T=
ENST00000652579.1:n.653T=
ENST00000652724.1:n.583T=
ENST00000332351.7:c.1378T= ENSP00000331327.3:p.Phe460=
ENST00000379077.7:c.*577T= ENSP00000368368.3:n.*577T=
ENST00000379079.6:c.742T= ENSP00000368370.2:p.Phe248=
ENST00000448076.7:c.1378T= ENSP00000413452.3:p.Phe460=
ENST00000452863.7:c.1327T= ENSP00000415516.3:p.Phe443=
ENST00000527882.5:c.359T=
ENST00000530998.5:c.691T= ENSP00000435307.1:p.Phe231=
NM_000378.4:c.1327T= NP_000369.3:p.Phe443=
NM_001198551.1:c.742T= , LRG_525t2:c.742T= NP_001185480.1:p.Phe248=
NM_001198552.1:c.691T= NP_001185481.1:p.Phe231=
NM_024424.3:c.1378T= NP_077742.2:p.Phe460=
NM_024426.4:c.1378T= NP_077744.3:p.Phe460=
NM_000378.5:c.1342T= NP_000369.4:p.Phe448=
NM_024424.4:c.1393T= NP_077742.3:p.Phe465=
NM_024426.5:c.1393T= NP_077744.4:p.Phe465=
NM_001367854.1:c.205T= NP_001354783.1:p.Phe69=
NR_160306.1:n.1725T=
NM_000378.6:c.1342T= NP_000369.4:p.Phe448=
NM_001198552.2:c.691T= NP_001185481.1:p.Phe231=
NM_024424.5:c.1393T= NP_077742.3:p.Phe465=
NM_024426.6:c.1393T= MANE Select NP_077744.4:p.Phe465=