Canonical Allele Identifier: CA936626186
Gene: WT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392021_32392027del , CM000673.2:g.32392021_32392027del GRCh38
NC_000011.9:g.32413567_32413573del , CM000673.1:g.32413567_32413573del GRCh37
NC_000011.8:g.32370143_32370149del NCBI36
NG_009272.1:g.48515_48521del , LRG_525:g.48515_48521del

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.1341_1347del ENSP00000331327.5:p.Lys447AsnfsTer6
ENST00000379077.9:c.*576_*582del ENSP00000368368.5:n.*576_*582del
ENST00000379079.8:c.741_747del ENSP00000368370.2:p.Lys247AsnfsTer6
ENST00000448076.9:c.1392_1398del ENSP00000413452.5:p.Lys464AsnfsTer6
ENST00000452863.10:c.1392_1398del MANE Select ENSP00000415516.5:p.Lys464AsnfsTer6
ENST00000526685.2:n.846_852del
ENST00000639563.3:c.1341_1347del ENSP00000492269.3:p.Lys447AsnfsTer6
ENST00000639907.2:n.535_541del
ENST00000640146.2:c.717_723del ENSP00000491984.2:p.Lys239AsnfsTer6
ENST00000650745.1:n.1202_1208del
ENST00000650861.1:n.1973_1979del
ENST00000650986.1:n.55_61del
ENST00000651459.1:c.163_169del
ENST00000651533.1:n.438_444del
ENST00000651668.1:n.329_335del
ENST00000651794.1:n.1235_1241del
ENST00000651819.1:n.317_323del
ENST00000652579.1:n.652_658del
ENST00000652724.1:n.582_588del
ENST00000332351.7:c.1377_1383del ENSP00000331327.3:p.Lys459AsnfsTer6
ENST00000379077.7:c.*576_*582del ENSP00000368368.3:n.*576_*582del
ENST00000379079.6:c.741_747del ENSP00000368370.2:p.Lys247AsnfsTer6
ENST00000448076.7:c.1377_1383del ENSP00000413452.3:p.Lys459AsnfsTer6
ENST00000452863.7:c.1326_1332del ENSP00000415516.3:p.Lys442AsnfsTer6
ENST00000527882.5:c.358_364del
ENST00000530998.5:c.690_696del ENSP00000435307.1:p.Lys230AsnfsTer6
NM_000378.4:c.1326_1332del NP_000369.3:p.Lys442AsnfsTer6
NM_001198551.1:c.741_747del , LRG_525t2:c.741_747del NP_001185480.1:p.Lys247AsnfsTer6
NM_001198552.1:c.690_696del NP_001185481.1:p.Lys230AsnfsTer6
NM_024424.3:c.1377_1383del NP_077742.2:p.Lys459AsnfsTer6
NM_024426.4:c.1377_1383del NP_077744.3:p.Lys459AsnfsTer6
NM_000378.5:c.1341_1347del NP_000369.4:p.Lys447AsnfsTer6
NM_024424.4:c.1392_1398del NP_077742.3:p.Lys464AsnfsTer6
NM_024426.5:c.1392_1398del NP_077744.4:p.Lys464AsnfsTer6
NM_001367854.1:c.204_210del NP_001354783.1:p.Lys68AsnfsTer6
NR_160306.1:n.1724_1730del
NM_000378.6:c.1341_1347del NP_000369.4:p.Lys447AsnfsTer6
NM_001198552.2:c.690_696del NP_001185481.1:p.Lys230AsnfsTer6
NM_024424.5:c.1392_1398del NP_077742.3:p.Lys464AsnfsTer6
NM_024426.6:c.1392_1398del MANE Select NP_077744.4:p.Lys464AsnfsTer6