Canonical Allele Identifier: CA1962335552
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392717G= , CM000673.2:g.32392717G= GRCh38
NC_000011.9:g.32414263G= , CM000673.1:g.32414263G= GRCh37
NC_000011.8:g.32370839G= NCBI36
NG_009272.1:g.47825C= , LRG_525:g.47825C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1252C= ENSP00000331327.5:p.Arg418=
ENST00000379077.9:c.*487C= ENSP00000368368.5:n.*487C=
ENST00000379079.8:c.652C= ENSP00000368370.2:p.Arg218=
ENST00000448076.9:c.1303C= ENSP00000413452.5:p.Arg435=
ENST00000452863.10:c.1303C= MANE Select ENSP00000415516.5:p.Arg435=
ENST00000526685.2:n.757C=
ENST00000639563.3:c.1252C= ENSP00000492269.3:p.Arg418=
ENST00000639907.2:n.446C=
ENST00000640146.2:c.628C= ENSP00000491984.2:p.Arg210=
ENST00000650745.1:n.512C=
ENST00000650861.1:n.1884C=
ENST00000651459.1:c.74C=
ENST00000651533.1:n.349C=
ENST00000651668.1:n.240C=
ENST00000651794.1:n.1146C=
ENST00000651819.1:n.228C=
ENST00000652579.1:n.563C=
ENST00000652724.1:n.493C=
ENST00000332351.7:c.1288C= ENSP00000331327.3:p.Arg430=
ENST00000379077.7:c.*487C= ENSP00000368368.3:n.*487C=
ENST00000379079.6:c.652C= ENSP00000368370.2:p.Arg218=
ENST00000448076.7:c.1288C= ENSP00000413452.3:p.Arg430=
ENST00000452863.7:c.1237C= ENSP00000415516.3:p.Arg413=
ENST00000527882.5:c.321-653C=
ENST00000530998.5:c.601C= ENSP00000435307.1:p.Arg201=
NM_000378.4:c.1237C= NP_000369.3:p.Arg413=
NM_001198551.1:c.652C= , LRG_525t2:c.652C= NP_001185480.1:p.Arg218=
NM_001198552.1:c.601C= NP_001185481.1:p.Arg201=
NM_024424.3:c.1288C= NP_077742.2:p.Arg430=
NM_024426.4:c.1288C= NP_077744.3:p.Arg430=
NM_000378.5:c.1252C= NP_000369.4:p.Arg418=
NM_024424.4:c.1303C= NP_077742.3:p.Arg435=
NM_024426.5:c.1303C= NP_077744.4:p.Arg435=
NM_001367854.1:c.115C= NP_001354783.1:p.Arg39=
NR_160306.1:n.1635C=
NM_000378.6:c.1252C= NP_000369.4:p.Arg418=
NM_001198552.2:c.601C= NP_001185481.1:p.Arg201=
NM_024424.5:c.1303C= NP_077742.3:p.Arg435=
NM_024426.6:c.1303C= MANE Select NP_077744.4:p.Arg435=