Canonical Allele Identifier: CA645577447
Gene: WT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392013dup , CM000673.2:g.32392013dup GRCh38
NC_000011.9:g.32413559dup , CM000673.1:g.32413559dup GRCh37
NC_000011.8:g.32370135dup NCBI36
NG_009272.1:g.48529dup , LRG_525:g.48529dup

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.1355dup ENSP00000331327.5:p.Asp452GlufsTer13
ENST00000379077.9:c.*590dup ENSP00000368368.5:n.*590dup
ENST00000379079.8:c.755dup ENSP00000368370.2:p.Asp252GlufsTer13
ENST00000448076.9:c.1406dup ENSP00000413452.5:p.Asp469GlufsTer13
ENST00000452863.10:c.1406dup MANE Select ENSP00000415516.5:p.Asp469GlufsTer13
ENST00000526685.2:n.860dup
ENST00000639563.3:c.1355dup ENSP00000492269.3:p.Asp452GlufsTer13
ENST00000639907.2:n.549dup
ENST00000640146.2:c.731dup ENSP00000491984.2:p.Asp244GlufsTer13
ENST00000650745.1:n.1216dup
ENST00000650861.1:n.1987dup
ENST00000650986.1:n.69dup
ENST00000651459.1:c.177dup
ENST00000651533.1:n.452dup
ENST00000651668.1:n.343dup
ENST00000651794.1:n.1249dup
ENST00000651819.1:n.331dup
ENST00000652579.1:n.666dup
ENST00000652724.1:n.596dup
ENST00000332351.7:c.1391dup ENSP00000331327.3:p.Asp464GlufsTer13
ENST00000379077.7:c.*590dup ENSP00000368368.3:n.*590dup
ENST00000379079.6:c.755dup ENSP00000368370.2:p.Asp252GlufsTer13
ENST00000448076.7:c.1391dup ENSP00000413452.3:p.Asp464GlufsTer13
ENST00000452863.7:c.1340dup ENSP00000415516.3:p.Asp447GlufsTer13
ENST00000527882.5:c.372dup
ENST00000530998.5:c.704dup ENSP00000435307.1:p.Asp235GlufsTer13
NM_000378.4:c.1340dup NP_000369.3:p.Asp447GlufsTer13
NM_001198551.1:c.755dup , LRG_525t2:c.755dup NP_001185480.1:p.Asp252GlufsTer13
NM_001198552.1:c.704dup NP_001185481.1:p.Asp235GlufsTer13
NM_024424.3:c.1391dup NP_077742.2:p.Asp464GlufsTer13
NM_024426.4:c.1391dup NP_077744.3:p.Asp464GlufsTer13
NM_000378.5:c.1355dup NP_000369.4:p.Asp452GlufsTer13
NM_024424.4:c.1406dup NP_077742.3:p.Asp469GlufsTer13
NM_024426.5:c.1406dup NP_077744.4:p.Asp469GlufsTer13
NM_001367854.1:c.218dup NP_001354783.1:p.Asp73GlufsTer13
NR_160306.1:n.1738dup
NM_000378.6:c.1355dup NP_000369.4:p.Asp452GlufsTer13
NM_001198552.2:c.704dup NP_001185481.1:p.Asp235GlufsTer13
NM_024424.5:c.1406dup NP_077742.3:p.Asp469GlufsTer13
NM_024426.6:c.1406dup MANE Select NP_077744.4:p.Asp469GlufsTer13