Canonical Allele Identifier: CA1962340649
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32400113A= , CM000673.2:g.32400113A= GRCh38
NC_000011.9:g.32421659A= , CM000673.1:g.32421659A= GRCh37
NC_000011.8:g.32378235A= NCBI36
NG_009272.1:g.40429T= , LRG_525:g.40429T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.966-69T= ENSP00000331327.5:n.966-69T=
ENST00000379077.9:c.*201-69T= ENSP00000368368.5:n.*201-69T=
ENST00000379079.8:c.366-69T= ENSP00000368370.2:n.366-69T=
ENST00000448076.9:c.1017-69T= ENSP00000413452.5:n.1017-69T=
ENST00000452863.10:c.1017-69T= MANE Select ENSP00000415516.5:n.1017-69T=
ENST00000526685.2:n.470+33T=
ENST00000639563.3:c.966-69T= ENSP00000492269.3:n.966-69T=
ENST00000639907.2:n.91T=
ENST00000640146.2:c.342-69T= ENSP00000491984.2:n.342-69T=
ENST00000651794.1:n.760-69T=
ENST00000652579.1:n.177-69T=
ENST00000652724.1:n.206+33T=
ENST00000332351.7:c.1002-69T= ENSP00000331327.3:n.1002-69T=
ENST00000379077.7:c.*201-69T= ENSP00000368368.3:n.*201-69T=
ENST00000379079.6:c.366-69T= ENSP00000368370.2:n.366-69T=
ENST00000448076.7:c.1002-69T= ENSP00000413452.3:n.1002-69T=
ENST00000452863.7:c.951-69T= ENSP00000415516.3:n.951-69T=
ENST00000526685.1:c.-173+33T= ENSP00000436292.1:n.-173+33T=
ENST00000527775.1:c.255-69T= ENSP00000435351.1:n.255-69T=
ENST00000527882.5:c.73-69T=
ENST00000530998.5:c.315-69T= ENSP00000435307.1:n.315-69T=
NM_000378.4:c.951-69T= NP_000369.3:n.951-69T=
NM_001198551.1:c.366-69T= , LRG_525t2:c.366-69T= NP_001185480.1:n.366-69T=
NM_001198552.1:c.315-69T= NP_001185481.1:n.315-69T=
NM_024424.3:c.1002-69T= NP_077742.2:n.1002-69T=
NM_024426.4:c.1002-69T= NP_077744.3:n.1002-69T=
NM_000378.5:c.966-69T= NP_000369.4:n.966-69T=
NM_024424.4:c.1017-69T= NP_077742.3:n.1017-69T=
NM_024426.5:c.1017-69T= NP_077744.4:n.1017-69T=
NM_001367854.1:c.-173+33T= NP_001354783.1:n.-173+33T=
NR_160306.1:n.1349-69T=
NM_000378.6:c.966-69T= NP_000369.4:n.966-69T=
NM_001198552.2:c.315-69T= NP_001185481.1:n.315-69T=
NM_024424.5:c.1017-69T= NP_077742.3:n.1017-69T=
NM_024426.6:c.1017-69T= MANE Select NP_077744.4:n.1017-69T=