Canonical Allele Identifier: CA2579961810
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32416528_32416529delinsAG , CM000673.2:g.32416528_32416529delinsAG GRCh38
NC_000011.9:g.32438074_32438075delinsAG , CM000673.1:g.32438074_32438075delinsAG GRCh37
NC_000011.8:g.32394650_32394651delinsAG NCBI36
NG_009272.1:g.24013_24014delinsCT , LRG_525:g.24013_24014delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.965+1048_965+1049delinsCT ENSP00000331327.5:n.965+1048_965+1049delinsCT
ENST00000379077.9:c.*161_*162delinsCT ENSP00000368368.5:n.*161_*162delinsCT
ENST00000379079.8:c.326_327delinsCT ENSP00000368370.2:p.Gly109Ala
ENST00000448076.9:c.977_978delinsCT ENSP00000413452.5:p.Gly326Ala
ENST00000452863.10:c.977_978delinsCT MANE Select ENSP00000415516.5:p.Gly326Ala
ENST00000639563.3:c.965+1048_965+1049delinsCT ENSP00000492269.3:n.965+1048_965+1049delinsCT
ENST00000640146.2:c.341+1048_341+1049delinsCT ENSP00000491984.2:n.341+1048_341+1049delinsCT
ENST00000651794.1:n.720_721delinsCT
ENST00000332351.7:c.962_963delinsCT ENSP00000331327.3:p.Gly321Ala
ENST00000379077.7:c.*161_*162delinsCT ENSP00000368368.3:n.*161_*162delinsCT
ENST00000379079.6:c.326_327delinsCT ENSP00000368370.2:p.Gly109Ala
ENST00000448076.7:c.962_963delinsCT ENSP00000413452.3:p.Gly321Ala
ENST00000452863.7:c.950+1048_950+1049delinsCT ENSP00000415516.3:n.950+1048_950+1049delinsCT
ENST00000527775.1:c.215_216delinsCT ENSP00000435351.1:p.Gly72Ala
ENST00000527882.5:c.33_34delinsCT
ENST00000530998.5:c.314+1048_314+1049delinsCT ENSP00000435307.1:n.314+1048_314+1049delinsCT
NM_000378.4:c.950+1048_950+1049delinsCT NP_000369.3:n.950+1048_950+1049delinsCT
NM_001198551.1:c.326_327delinsCT , LRG_525t2:c.326_327delinsCT NP_001185480.1:p.Gly109Ala
NM_001198552.1:c.314+1048_314+1049delinsCT NP_001185481.1:n.314+1048_314+1049delinsCT
NM_024424.3:c.962_963delinsCT NP_077742.2:p.Gly321Ala
NM_024426.4:c.962_963delinsCT NP_077744.3:p.Gly321Ala
NM_000378.5:c.965+1048_965+1049delinsCT NP_000369.4:n.965+1048_965+1049delinsCT
NM_024424.4:c.977_978delinsCT NP_077742.3:p.Gly326Ala
NM_024426.5:c.977_978delinsCT NP_077744.4:p.Gly326Ala
NR_160306.1:n.1309_1310delinsCT
NM_000378.6:c.965+1048_965+1049delinsCT NP_000369.4:n.965+1048_965+1049delinsCT
NM_001198552.2:c.314+1048_314+1049delinsCT NP_001185481.1:n.314+1048_314+1049delinsCT
NM_024424.5:c.977_978delinsCT NP_077742.3:p.Gly326Ala
NM_024426.6:c.977_978delinsCT MANE Select NP_077744.4:p.Gly326Ala