Canonical Allele Identifier: CA1962335255
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392000G= , CM000673.2:g.32392000G= GRCh38
NC_000011.9:g.32413546G= , CM000673.1:g.32413546G= GRCh37
NC_000011.8:g.32370122G= NCBI36
NG_009272.1:g.48542C= , LRG_525:g.48542C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1368C= ENSP00000331327.5:p.Thr456=
ENST00000379077.9:c.*603C= ENSP00000368368.5:n.*603C=
ENST00000379079.8:c.768C= ENSP00000368370.2:p.Thr256=
ENST00000448076.9:c.1419C= ENSP00000413452.5:p.Thr473=
ENST00000452863.10:c.1419C= MANE Select ENSP00000415516.5:p.Thr473=
ENST00000526685.2:n.873C=
ENST00000639563.3:c.1368C= ENSP00000492269.3:p.Thr456=
ENST00000639907.2:n.562C=
ENST00000640146.2:c.744C= ENSP00000491984.2:p.Thr248=
ENST00000650745.1:n.1229C=
ENST00000650861.1:n.2000C=
ENST00000650986.1:n.82C=
ENST00000651459.1:c.190C=
ENST00000651533.1:n.465C=
ENST00000651668.1:n.356C=
ENST00000651794.1:n.1262C=
ENST00000651819.1:n.344C=
ENST00000652579.1:n.679C=
ENST00000652724.1:n.609C=
ENST00000332351.7:c.1404C= ENSP00000331327.3:p.Thr468=
ENST00000379077.7:c.*603C= ENSP00000368368.3:n.*603C=
ENST00000379079.6:c.768C= ENSP00000368370.2:p.Thr256=
ENST00000448076.7:c.1404C= ENSP00000413452.3:p.Thr468=
ENST00000452863.7:c.1353C= ENSP00000415516.3:p.Thr451=
ENST00000527882.5:c.385C=
ENST00000530998.5:c.717C= ENSP00000435307.1:p.Thr239=
NM_000378.4:c.1353C= NP_000369.3:p.Thr451=
NM_001198551.1:c.768C= , LRG_525t2:c.768C= NP_001185480.1:p.Thr256=
NM_001198552.1:c.717C= NP_001185481.1:p.Thr239=
NM_024424.3:c.1404C= NP_077742.2:p.Thr468=
NM_024426.4:c.1404C= NP_077744.3:p.Thr468=
NM_000378.5:c.1368C= NP_000369.4:p.Thr456=
NM_024424.4:c.1419C= NP_077742.3:p.Thr473=
NM_024426.5:c.1419C= NP_077744.4:p.Thr473=
NM_001367854.1:c.231C= NP_001354783.1:p.Thr77=
NR_160306.1:n.1751C=
NM_000378.6:c.1368C= NP_000369.4:p.Thr456=
NM_001198552.2:c.717C= NP_001185481.1:p.Thr239=
NM_024424.5:c.1419C= NP_077742.3:p.Thr473=
NM_024426.6:c.1419C= MANE Select NP_077744.4:p.Thr473=