Canonical Allele Identifier: CA1962335272
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392020G= , CM000673.2:g.32392020G= GRCh38
NC_000011.9:g.32413566G= , CM000673.1:g.32413566G= GRCh37
NC_000011.8:g.32370142G= NCBI36
NG_009272.1:g.48522C= , LRG_525:g.48522C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1348C= ENSP00000331327.5:p.Arg450=
ENST00000379077.9:c.*583C= ENSP00000368368.5:n.*583C=
ENST00000379079.8:c.748C= ENSP00000368370.2:p.Arg250=
ENST00000448076.9:c.1399C= ENSP00000413452.5:p.Arg467=
ENST00000452863.10:c.1399C= MANE Select ENSP00000415516.5:p.Arg467=
ENST00000526685.2:n.853C=
ENST00000639563.3:c.1348C= ENSP00000492269.3:p.Arg450=
ENST00000639907.2:n.542C=
ENST00000640146.2:c.724C= ENSP00000491984.2:p.Arg242=
ENST00000650745.1:n.1209C=
ENST00000650861.1:n.1980C=
ENST00000650986.1:n.62C=
ENST00000651459.1:c.170C=
ENST00000651533.1:n.445C=
ENST00000651668.1:n.336C=
ENST00000651794.1:n.1242C=
ENST00000651819.1:n.324C=
ENST00000652579.1:n.659C=
ENST00000652724.1:n.589C=
ENST00000332351.7:c.1384C= ENSP00000331327.3:p.Arg462=
ENST00000379077.7:c.*583C= ENSP00000368368.3:n.*583C=
ENST00000379079.6:c.748C= ENSP00000368370.2:p.Arg250=
ENST00000448076.7:c.1384C= ENSP00000413452.3:p.Arg462=
ENST00000452863.7:c.1333C= ENSP00000415516.3:p.Arg445=
ENST00000527882.5:c.365C=
ENST00000530998.5:c.697C= ENSP00000435307.1:p.Arg233=
NM_000378.4:c.1333C= NP_000369.3:p.Arg445=
NM_001198551.1:c.748C= , LRG_525t2:c.748C= NP_001185480.1:p.Arg250=
NM_001198552.1:c.697C= NP_001185481.1:p.Arg233=
NM_024424.3:c.1384C= NP_077742.2:p.Arg462=
NM_024426.4:c.1384C= NP_077744.3:p.Arg462=
NM_000378.5:c.1348C= NP_000369.4:p.Arg450=
NM_024424.4:c.1399C= NP_077742.3:p.Arg467=
NM_024426.5:c.1399C= NP_077744.4:p.Arg467=
NM_001367854.1:c.211C= NP_001354783.1:p.Arg71=
NR_160306.1:n.1731C=
NM_000378.6:c.1348C= NP_000369.4:p.Arg450=
NM_001198552.2:c.697C= NP_001185481.1:p.Arg233=
NM_024424.5:c.1399C= NP_077742.3:p.Arg467=
NM_024426.6:c.1399C= MANE Select NP_077744.4:p.Arg467=