Canonical Allele Identifier: CA1962335548
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392705G= , CM000673.2:g.32392705G= GRCh38
NC_000011.9:g.32414251G= , CM000673.1:g.32414251G= GRCh37
NC_000011.8:g.32370827G= NCBI36
NG_009272.1:g.47837C= , LRG_525:g.47837C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1264C= ENSP00000331327.5:p.Arg422=
ENST00000379077.9:c.*499C= ENSP00000368368.5:n.*499C=
ENST00000379079.8:c.664C= ENSP00000368370.2:p.Arg222=
ENST00000448076.9:c.1315C= ENSP00000413452.5:p.Arg439=
ENST00000452863.10:c.1315C= MANE Select ENSP00000415516.5:p.Arg439=
ENST00000526685.2:n.769C=
ENST00000639563.3:c.1264C= ENSP00000492269.3:p.Arg422=
ENST00000639907.2:n.458C=
ENST00000640146.2:c.640C= ENSP00000491984.2:p.Arg214=
ENST00000650745.1:n.524C=
ENST00000650861.1:n.1896C=
ENST00000651459.1:c.86C=
ENST00000651533.1:n.361C=
ENST00000651668.1:n.252C=
ENST00000651794.1:n.1158C=
ENST00000651819.1:n.240C=
ENST00000652579.1:n.575C=
ENST00000652724.1:n.505C=
ENST00000332351.7:c.1300C= ENSP00000331327.3:p.Arg434=
ENST00000379077.7:c.*499C= ENSP00000368368.3:n.*499C=
ENST00000379079.6:c.664C= ENSP00000368370.2:p.Arg222=
ENST00000448076.7:c.1300C= ENSP00000413452.3:p.Arg434=
ENST00000452863.7:c.1249C= ENSP00000415516.3:p.Arg417=
ENST00000527882.5:c.321-641C=
ENST00000530998.5:c.613C= ENSP00000435307.1:p.Arg205=
NM_000378.4:c.1249C= NP_000369.3:p.Arg417=
NM_001198551.1:c.664C= , LRG_525t2:c.664C= NP_001185480.1:p.Arg222=
NM_001198552.1:c.613C= NP_001185481.1:p.Arg205=
NM_024424.3:c.1300C= NP_077742.2:p.Arg434=
NM_024426.4:c.1300C= NP_077744.3:p.Arg434=
NM_000378.5:c.1264C= NP_000369.4:p.Arg422=
NM_024424.4:c.1315C= NP_077742.3:p.Arg439=
NM_024426.5:c.1315C= NP_077744.4:p.Arg439=
NM_001367854.1:c.127C= NP_001354783.1:p.Arg43=
NR_160306.1:n.1647C=
NM_000378.6:c.1264C= NP_000369.4:p.Arg422=
NM_001198552.2:c.613C= NP_001185481.1:p.Arg205=
NM_024424.5:c.1315C= NP_077742.3:p.Arg439=
NM_024426.6:c.1315C= MANE Select NP_077744.4:p.Arg439=