Canonical Allele Identifier: CA1962340472
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32400022C= , CM000673.2:g.32400022C= GRCh38
NC_000011.9:g.32421568C= , CM000673.1:g.32421568C= GRCh37
NC_000011.8:g.32378144C= NCBI36
NG_009272.1:g.40520G= , LRG_525:g.40520G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.988G= ENSP00000331327.5:p.Asp330=
ENST00000379077.9:c.*223G= ENSP00000368368.5:n.*223G=
ENST00000379079.8:c.388G= ENSP00000368370.2:p.Asp130=
ENST00000448076.9:c.1039G= ENSP00000413452.5:p.Asp347=
ENST00000452863.10:c.1039G= MANE Select ENSP00000415516.5:p.Asp347=
ENST00000526685.2:n.493G=
ENST00000639563.3:c.988G= ENSP00000492269.3:p.Asp330=
ENST00000639907.2:n.182G=
ENST00000640146.2:c.364G= ENSP00000491984.2:p.Asp122=
ENST00000651794.1:n.782G=
ENST00000652579.1:n.199G=
ENST00000652724.1:n.229G=
ENST00000332351.7:c.1024G= ENSP00000331327.3:p.Asp342=
ENST00000379077.7:c.*223G= ENSP00000368368.3:n.*223G=
ENST00000379079.6:c.388G= ENSP00000368370.2:p.Asp130=
ENST00000448076.7:c.1024G= ENSP00000413452.3:p.Asp342=
ENST00000452863.7:c.973G= ENSP00000415516.3:p.Asp325=
ENST00000526685.1:c.-150G= ENSP00000436292.1:n.-150G=
ENST00000527775.1:c.277G= ENSP00000435351.1:p.Asp93=
ENST00000527882.5:c.95G=
ENST00000530998.5:c.337G= ENSP00000435307.1:p.Asp113=
NM_000378.4:c.973G= NP_000369.3:p.Asp325=
NM_001198551.1:c.388G= , LRG_525t2:c.388G= NP_001185480.1:p.Asp130=
NM_001198552.1:c.337G= NP_001185481.1:p.Asp113=
NM_024424.3:c.1024G= NP_077742.2:p.Asp342=
NM_024426.4:c.1024G= NP_077744.3:p.Asp342=
NM_000378.5:c.988G= NP_000369.4:p.Asp330=
NM_024424.4:c.1039G= NP_077742.3:p.Asp347=
NM_024426.5:c.1039G= NP_077744.4:p.Asp347=
NM_001367854.1:c.-150G= NP_001354783.1:n.-150G=
NR_160306.1:n.1371G=
NM_000378.6:c.988G= NP_000369.4:p.Asp330=
NM_001198552.2:c.337G= NP_001185481.1:p.Asp113=
NM_024424.5:c.1039G= NP_077742.3:p.Asp347=
NM_024426.6:c.1039G= MANE Select NP_077744.4:p.Asp347=