Canonical Allele Identifier: CA936626227
Gene: WT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32392030_32392031insAAAAAAT , CM000673.2:g.32392030_32392031insAAAAAAT GRCh38
NC_000011.9:g.32413576_32413577insAAAAAAT , CM000673.1:g.32413576_32413577insAAAAAAT GRCh37
NC_000011.8:g.32370152_32370153insAAAAAAT NCBI36
NG_009272.1:g.48512_48513insTTTTTTA , LRG_525:g.48512_48513insTTTTTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.1338_1339insTTTTTTA ENSP00000331327.5:p.Lys447PhefsTer20
ENST00000379077.9:c.*573_*574insTTTTTTA ENSP00000368368.5:n.*573_*574insTTTTTTA
ENST00000379079.8:c.738_739insTTTTTTA ENSP00000368370.2:p.Lys247PhefsTer20
ENST00000448076.9:c.1389_1390insTTTTTTA ENSP00000413452.5:p.Lys464PhefsTer20
ENST00000452863.10:c.1389_1390insTTTTTTA MANE Select ENSP00000415516.5:p.Lys464PhefsTer20
ENST00000526685.2:n.843_844insTTTTTTA
ENST00000639563.3:c.1338_1339insTTTTTTA ENSP00000492269.3:p.Lys447PhefsTer20
ENST00000639907.2:n.532_533insTTTTTTA
ENST00000640146.2:c.714_715insTTTTTTA ENSP00000491984.2:p.Lys239PhefsTer20
ENST00000650745.1:n.1199_1200insTTTTTTA
ENST00000650861.1:n.1970_1971insTTTTTTA
ENST00000650986.1:n.52_53insTTTTTTA
ENST00000651459.1:c.160_161insTTTTTTA
ENST00000651533.1:n.435_436insTTTTTTA
ENST00000651668.1:n.326_327insTTTTTTA
ENST00000651794.1:n.1232_1233insTTTTTTA
ENST00000651819.1:n.314_315insTTTTTTA
ENST00000652579.1:n.649_650insTTTTTTA
ENST00000652724.1:n.579_580insTTTTTTA
ENST00000332351.7:c.1374_1375insTTTTTTA ENSP00000331327.3:p.Lys459PhefsTer20
ENST00000379077.7:c.*573_*574insTTTTTTA ENSP00000368368.3:n.*573_*574insTTTTTTA
ENST00000379079.6:c.738_739insTTTTTTA ENSP00000368370.2:p.Lys247PhefsTer20
ENST00000448076.7:c.1374_1375insTTTTTTA ENSP00000413452.3:p.Lys459PhefsTer20
ENST00000452863.7:c.1323_1324insTTTTTTA ENSP00000415516.3:p.Lys442PhefsTer20
ENST00000527882.5:c.355_356insTTTTTTA
ENST00000530998.5:c.687_688insTTTTTTA ENSP00000435307.1:p.Lys230PhefsTer20
NM_000378.4:c.1323_1324insTTTTTTA NP_000369.3:p.Lys442PhefsTer20
NM_001198551.1:c.738_739insTTTTTTA , LRG_525t2:c.738_739insTTTTTTA NP_001185480.1:p.Lys247PhefsTer20
NM_001198552.1:c.687_688insTTTTTTA NP_001185481.1:p.Lys230PhefsTer20
NM_024424.3:c.1374_1375insTTTTTTA NP_077742.2:p.Lys459PhefsTer20
NM_024426.4:c.1374_1375insTTTTTTA NP_077744.3:p.Lys459PhefsTer20
NM_000378.5:c.1338_1339insTTTTTTA NP_000369.4:p.Lys447PhefsTer20
NM_024424.4:c.1389_1390insTTTTTTA NP_077742.3:p.Lys464PhefsTer20
NM_024426.5:c.1389_1390insTTTTTTA NP_077744.4:p.Lys464PhefsTer20
NM_001367854.1:c.201_202insTTTTTTA NP_001354783.1:p.Lys68PhefsTer20
NR_160306.1:n.1721_1722insTTTTTTA
NM_000378.6:c.1338_1339insTTTTTTA NP_000369.4:p.Lys447PhefsTer20
NM_001198552.2:c.687_688insTTTTTTA NP_001185481.1:p.Lys230PhefsTer20
NM_024424.5:c.1389_1390insTTTTTTA NP_077742.3:p.Lys464PhefsTer20
NM_024426.6:c.1389_1390insTTTTTTA MANE Select NP_077744.4:p.Lys464PhefsTer20