Canonical Allele Identifier: CA2723459242
Gene: WT1 HGNC NCBI

Linked Data

dbSNP Id: rs2132919890

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392690del , CM000673.2:g.32392690del GRCh38
NC_000011.9:g.32414236del , CM000673.1:g.32414236del GRCh37
NC_000011.8:g.32370812del NCBI36
NG_009272.1:g.47855del , LRG_525:g.47855del

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.1282del ENSP00000331327.5:p.Arg428AspfsTer9
ENST00000379077.9:c.*517del ENSP00000368368.5:n.*517del
ENST00000379079.8:c.682del ENSP00000368370.2:p.Arg228AspfsTer9
ENST00000448076.9:c.1333del ENSP00000413452.5:p.Arg445AspfsTer9
ENST00000452863.10:c.1333del MANE Select ENSP00000415516.5:p.Arg445AspfsTer9
ENST00000526685.2:n.787del
ENST00000639563.3:c.1282del ENSP00000492269.3:p.Arg428AspfsTer9
ENST00000639907.2:n.476del
ENST00000640146.2:c.658del ENSP00000491984.2:p.Arg220AspfsTer9
ENST00000650745.1:n.542del
ENST00000650861.1:n.1914del
ENST00000651459.1:c.104del
ENST00000651533.1:n.379del
ENST00000651668.1:n.270del
ENST00000651794.1:n.1176del
ENST00000651819.1:n.258del
ENST00000652579.1:n.593del
ENST00000652724.1:n.523del
ENST00000332351.7:c.1318del ENSP00000331327.3:p.Arg440AspfsTer9
ENST00000379077.7:c.*517del ENSP00000368368.3:n.*517del
ENST00000379079.6:c.682del ENSP00000368370.2:p.Arg228AspfsTer9
ENST00000448076.7:c.1318del ENSP00000413452.3:p.Arg440AspfsTer9
ENST00000452863.7:c.1267del ENSP00000415516.3:p.Arg423AspfsTer9
ENST00000527882.5:c.321-623del
ENST00000530998.5:c.631del ENSP00000435307.1:p.Arg211AspfsTer9
NM_000378.4:c.1267del NP_000369.3:p.Arg423AspfsTer9
NM_001198551.1:c.682del , LRG_525t2:c.682del NP_001185480.1:p.Arg228AspfsTer9
NM_001198552.1:c.631del NP_001185481.1:p.Arg211AspfsTer9
NM_024424.3:c.1318del NP_077742.2:p.Arg440AspfsTer9
NM_024426.4:c.1318del NP_077744.3:p.Arg440AspfsTer9
NM_000378.5:c.1282del NP_000369.4:p.Arg428AspfsTer9
NM_024424.4:c.1333del NP_077742.3:p.Arg445AspfsTer9
NM_024426.5:c.1333del NP_077744.4:p.Arg445AspfsTer9
NM_001367854.1:c.145del NP_001354783.1:p.Arg49AspfsTer9
NR_160306.1:n.1665del
NM_000378.6:c.1282del NP_000369.4:p.Arg428AspfsTer9
NM_001198552.2:c.631del NP_001185481.1:p.Arg211AspfsTer9
NM_024424.5:c.1333del NP_077742.3:p.Arg445AspfsTer9
NM_024426.6:c.1333del MANE Select NP_077744.4:p.Arg445AspfsTer9