Canonical Allele Identifier: CA1962335544
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392682G= , CM000673.2:g.32392682G= GRCh38
NC_000011.9:g.32414228G= , CM000673.1:g.32414228G= GRCh37
NC_000011.8:g.32370804G= NCBI36
NG_009272.1:g.47860C= , LRG_525:g.47860C=

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.1287C= ENSP00000331327.5:p.His429=
ENST00000379077.9:c.*522C= ENSP00000368368.5:n.*522C=
ENST00000379079.8:c.687C= ENSP00000368370.2:p.His229=
ENST00000448076.9:c.1338C= ENSP00000413452.5:p.His446=
ENST00000452863.10:c.1338C= MANE Select ENSP00000415516.5:p.His446=
ENST00000526685.2:n.792C=
ENST00000639563.3:c.1287C= ENSP00000492269.3:p.His429=
ENST00000639907.2:n.481C=
ENST00000640146.2:c.663C= ENSP00000491984.2:p.His221=
ENST00000650745.1:n.547C=
ENST00000650861.1:n.1919C=
ENST00000651459.1:c.109C=
ENST00000651533.1:n.384C=
ENST00000651668.1:n.275C=
ENST00000651794.1:n.1181C=
ENST00000651819.1:n.263C=
ENST00000652579.1:n.598C=
ENST00000652724.1:n.528C=
ENST00000332351.7:c.1323C= ENSP00000331327.3:p.His441=
ENST00000379077.7:c.*522C= ENSP00000368368.3:n.*522C=
ENST00000379079.6:c.687C= ENSP00000368370.2:p.His229=
ENST00000448076.7:c.1323C= ENSP00000413452.3:p.His441=
ENST00000452863.7:c.1272C= ENSP00000415516.3:p.His424=
ENST00000527882.5:c.321-618C=
ENST00000530998.5:c.636C= ENSP00000435307.1:p.His212=
NM_000378.4:c.1272C= NP_000369.3:p.His424=
NM_001198551.1:c.687C= , LRG_525t2:c.687C= NP_001185480.1:p.His229=
NM_001198552.1:c.636C= NP_001185481.1:p.His212=
NM_024424.3:c.1323C= NP_077742.2:p.His441=
NM_024426.4:c.1323C= NP_077744.3:p.His441=
NM_000378.5:c.1287C= NP_000369.4:p.His429=
NM_024424.4:c.1338C= NP_077742.3:p.His446=
NM_024426.5:c.1338C= NP_077744.4:p.His446=
NM_001367854.1:c.150C= NP_001354783.1:p.His50=
NR_160306.1:n.1670C=
NM_000378.6:c.1287C= NP_000369.4:p.His429=
NM_001198552.2:c.636C= NP_001185481.1:p.His212=
NM_024424.5:c.1338C= NP_077742.3:p.His446=
NM_024426.6:c.1338C= MANE Select NP_077744.4:p.His446=