Canonical Allele Identifier: CA2612972938
Gene: WT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392598del , CM000673.2:g.32392598del GRCh38
NC_000011.9:g.32414144del , CM000673.1:g.32414144del GRCh37
NC_000011.8:g.32370720del NCBI36
NG_009272.1:g.47944del , LRG_525:g.47944del

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1303+68del ENSP00000331327.5:n.1303+68del
ENST00000379077.9:c.*538+68del ENSP00000368368.5:n.*538+68del
ENST00000379079.8:c.703+68del ENSP00000368370.2:n.703+68del
ENST00000448076.9:c.1354+68del ENSP00000413452.5:n.1354+68del
ENST00000452863.10:c.1354+68del MANE Select ENSP00000415516.5:n.1354+68del
ENST00000526685.2:n.808+68del
ENST00000639563.3:c.1303+68del ENSP00000492269.3:n.1303+68del
ENST00000639907.2:n.497+68del
ENST00000640146.2:c.679+68del ENSP00000491984.2:n.679+68del
ENST00000650745.1:n.631del
ENST00000650861.1:n.1935+68del
ENST00000651459.1:c.125+68del
ENST00000651533.1:n.400+68del
ENST00000651668.1:n.291+68del
ENST00000651794.1:n.1197+68del
ENST00000651819.1:n.279+68del
ENST00000652579.1:n.614+68del
ENST00000652724.1:n.544+68del
ENST00000332351.7:c.1339+68del ENSP00000331327.3:n.1339+68del
ENST00000379077.7:c.*538+68del ENSP00000368368.3:n.*538+68del
ENST00000379079.6:c.703+68del ENSP00000368370.2:n.703+68del
ENST00000448076.7:c.1339+68del ENSP00000413452.3:n.1339+68del
ENST00000452863.7:c.1288+68del ENSP00000415516.3:n.1288+68del
ENST00000527882.5:c.321-534del
ENST00000530998.5:c.652+68del ENSP00000435307.1:n.652+68del
NM_000378.4:c.1288+68del NP_000369.3:n.1288+68del
NM_001198551.1:c.703+68del , LRG_525t2:c.703+68del NP_001185480.1:n.703+68del
NM_001198552.1:c.652+68del NP_001185481.1:n.652+68del
NM_024424.3:c.1339+68del NP_077742.2:n.1339+68del
NM_024426.4:c.1339+68del NP_077744.3:n.1339+68del
NM_000378.5:c.1303+68del NP_000369.4:n.1303+68del
NM_024424.4:c.1354+68del NP_077742.3:n.1354+68del
NM_024426.5:c.1354+68del NP_077744.4:n.1354+68del
NM_001367854.1:c.166+68del NP_001354783.1:n.166+68del
NR_160306.1:n.1686+68del
NM_000378.6:c.1303+68del NP_000369.4:n.1303+68del
NM_001198552.2:c.652+68del NP_001185481.1:n.652+68del
NM_024424.5:c.1354+68del NP_077742.3:n.1354+68del
NM_024426.6:c.1354+68del MANE Select NP_077744.4:n.1354+68del