Canonical Allele Identifier: CA2695202575
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392681G= , CM000673.2:g.32392681G= GRCh38
NC_000011.9:g.32414227G= , CM000673.1:g.32414227G= GRCh37
NC_000011.8:g.32370803G= NCBI36
NG_009272.1:g.47861C= , LRG_525:g.47861C=

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.1288C= ENSP00000331327.5:p.Gln430=
ENST00000379077.9:c.*523C= ENSP00000368368.5:n.*523C=
ENST00000379079.8:c.688C= ENSP00000368370.2:p.Gln230=
ENST00000448076.9:c.1339C= ENSP00000413452.5:p.Gln447=
ENST00000452863.10:c.1339C= MANE Select ENSP00000415516.5:p.Gln447=
ENST00000526685.2:n.793C=
ENST00000639563.3:c.1288C= ENSP00000492269.3:p.Gln430=
ENST00000639907.2:n.482C=
ENST00000640146.2:c.664C= ENSP00000491984.2:p.Gln222=
ENST00000650745.1:n.548C=
ENST00000650861.1:n.1920C=
ENST00000651459.1:c.110C=
ENST00000651533.1:n.385C=
ENST00000651668.1:n.276C=
ENST00000651794.1:n.1182C=
ENST00000651819.1:n.264C=
ENST00000652579.1:n.599C=
ENST00000652724.1:n.529C=
ENST00000332351.7:c.1324C= ENSP00000331327.3:p.Gln442=
ENST00000379077.7:c.*523C= ENSP00000368368.3:n.*523C=
ENST00000379079.6:c.688C= ENSP00000368370.2:p.Gln230=
ENST00000448076.7:c.1324C= ENSP00000413452.3:p.Gln442=
ENST00000452863.7:c.1273C= ENSP00000415516.3:p.Gln425=
ENST00000527882.5:c.321-617C=
ENST00000530998.5:c.637C= ENSP00000435307.1:p.Gln213=
NM_000378.4:c.1273C= NP_000369.3:p.Gln425=
NM_001198551.1:c.688C= , LRG_525t2:c.688C= NP_001185480.1:p.Gln230=
NM_001198552.1:c.637C= NP_001185481.1:p.Gln213=
NM_024424.3:c.1324C= NP_077742.2:p.Gln442=
NM_024426.4:c.1324C= NP_077744.3:p.Gln442=
NM_000378.5:c.1288C= NP_000369.4:p.Gln430=
NM_024424.4:c.1339C= NP_077742.3:p.Gln447=
NM_024426.5:c.1339C= NP_077744.4:p.Gln447=
NM_001367854.1:c.151C= NP_001354783.1:p.Gln51=
NR_160306.1:n.1671C=
NM_000378.6:c.1288C= NP_000369.4:p.Gln430=
NM_001198552.2:c.637C= NP_001185481.1:p.Gln213=
NM_024424.5:c.1339C= NP_077742.3:p.Gln447=
NM_024426.6:c.1339C= MANE Select NP_077744.4:p.Gln447=