Canonical Allele Identifier: CA2695202602
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392014_32392015delinsTC , CM000673.2:g.32392014_32392015delinsTC GRCh38
NC_000011.9:g.32413560_32413561delinsTC , CM000673.1:g.32413560_32413561delinsTC GRCh37
NC_000011.8:g.32370136_32370137delinsTC NCBI36
NG_009272.1:g.48527_48528delinsGA , LRG_525:g.48527_48528delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1353_1354delinsGA ENSP00000331327.5:p.Asp452Asn
ENST00000379077.9:c.*588_*589delinsGA ENSP00000368368.5:n.*588_*589delinsGA
ENST00000379079.8:c.753_754delinsGA ENSP00000368370.2:p.Asp252Asn
ENST00000448076.9:c.1404_1405delinsGA ENSP00000413452.5:p.Asp469Asn
ENST00000452863.10:c.1404_1405delinsGA MANE Select ENSP00000415516.5:p.Asp469Asn
ENST00000526685.2:n.858_859delinsGA
ENST00000639563.3:c.1353_1354delinsGA ENSP00000492269.3:p.Asp452Asn
ENST00000639907.2:n.547_548delinsGA
ENST00000640146.2:c.729_730delinsGA ENSP00000491984.2:p.Asp244Asn
ENST00000650745.1:n.1214_1215delinsGA
ENST00000650861.1:n.1985_1986delinsGA
ENST00000650986.1:n.67_68delinsGA
ENST00000651459.1:c.175_176delinsGA
ENST00000651533.1:n.450_451delinsGA
ENST00000651668.1:n.341_342delinsGA
ENST00000651794.1:n.1247_1248delinsGA
ENST00000651819.1:n.329_330delinsGA
ENST00000652579.1:n.664_665delinsGA
ENST00000652724.1:n.594_595delinsGA
ENST00000332351.7:c.1389_1390delinsGA ENSP00000331327.3:p.Asp464Asn
ENST00000379077.7:c.*588_*589delinsGA ENSP00000368368.3:n.*588_*589delinsGA
ENST00000379079.6:c.753_754delinsGA ENSP00000368370.2:p.Asp252Asn
ENST00000448076.7:c.1389_1390delinsGA ENSP00000413452.3:p.Asp464Asn
ENST00000452863.7:c.1338_1339delinsGA ENSP00000415516.3:p.Asp447Asn
ENST00000527882.5:c.370_371delinsGA
ENST00000530998.5:c.702_703delinsGA ENSP00000435307.1:p.Asp235Asn
NM_000378.4:c.1338_1339delinsGA NP_000369.3:p.Asp447Asn
NM_001198551.1:c.753_754delinsGA , LRG_525t2:c.753_754delinsGA NP_001185480.1:p.Asp252Asn
NM_001198552.1:c.702_703delinsGA NP_001185481.1:p.Asp235Asn
NM_024424.3:c.1389_1390delinsGA NP_077742.2:p.Asp464Asn
NM_024426.4:c.1389_1390delinsGA NP_077744.3:p.Asp464Asn
NM_000378.5:c.1353_1354delinsGA NP_000369.4:p.Asp452Asn
NM_024424.4:c.1404_1405delinsGA NP_077742.3:p.Asp469Asn
NM_024426.5:c.1404_1405delinsGA NP_077744.4:p.Asp469Asn
NM_001367854.1:c.216_217delinsGA NP_001354783.1:p.Asp73Asn
NR_160306.1:n.1736_1737delinsGA
NM_000378.6:c.1353_1354delinsGA NP_000369.4:p.Asp452Asn
NM_001198552.2:c.702_703delinsGA NP_001185481.1:p.Asp235Asn
NM_024424.5:c.1404_1405delinsGA NP_077742.3:p.Asp469Asn
NM_024426.6:c.1404_1405delinsGA MANE Select NP_077744.4:p.Asp469Asn