Canonical Allele Identifier: CA2790961093

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392033_32392034insATTAAAAAAAAAA , CM000673.2:g.32392033_32392034insATTAAAAAAAAAA	GRCh38
NC_000011.9:g.32413579_32413580insATTAAAAAAAAAA , CM000673.1:g.32413579_32413580insATTAAAAAAAAAA	GRCh37
NC_000011.8:g.32370155_32370156insATTAAAAAAAAAA	NCBI36
NG_009272.1:g.48508_48509insTTTTTTTTTTAAT , LRG_525:g.48508_48509insTTTTTTTTTTAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1334_1335insTTTTTTTTTTAAT	ENSP00000331327.5:p.Gln445HisfsTer24
ENST00000379077.9:c.*569_*570insTTTTTTTTTTAAT	ENSP00000368368.5:n.*569_*570insTTTTTTTTTTAAT
ENST00000379079.8:c.734_735insTTTTTTTTTTAAT	ENSP00000368370.2:p.Gln245HisfsTer24
ENST00000448076.9:c.1385_1386insTTTTTTTTTTAAT	ENSP00000413452.5:p.Gln462HisfsTer24
ENST00000452863.10:c.1385_1386insTTTTTTTTTTAAT MANE Select	ENSP00000415516.5:p.Gln462HisfsTer24
ENST00000526685.2:n.839_840insTTTTTTTTTTAAT
ENST00000639563.3:c.1334_1335insTTTTTTTTTTAAT	ENSP00000492269.3:p.Gln445HisfsTer24
ENST00000639907.2:n.528_529insTTTTTTTTTTAAT
ENST00000640146.2:c.710_711insTTTTTTTTTTAAT	ENSP00000491984.2:p.Gln237HisfsTer24
ENST00000650745.1:n.1195_1196insTTTTTTTTTTAAT
ENST00000650861.1:n.1966_1967insTTTTTTTTTTAAT
ENST00000650986.1:n.48_49insTTTTTTTTTTAAT
ENST00000651459.1:c.156_157insTTTTTTTTTTAAT
ENST00000651533.1:n.431_432insTTTTTTTTTTAAT
ENST00000651668.1:n.322_323insTTTTTTTTTTAAT
ENST00000651794.1:n.1228_1229insTTTTTTTTTTAAT
ENST00000651819.1:n.310_311insTTTTTTTTTTAAT
ENST00000652579.1:n.645_646insTTTTTTTTTTAAT
ENST00000652724.1:n.575_576insTTTTTTTTTTAAT
ENST00000332351.7:c.1370_1371insTTTTTTTTTTAAT	ENSP00000331327.3:p.Gln457HisfsTer24
ENST00000379077.7:c.*569_*570insTTTTTTTTTTAAT	ENSP00000368368.3:n.*569_*570insTTTTTTTTTTAAT
ENST00000379079.6:c.734_735insTTTTTTTTTTAAT	ENSP00000368370.2:p.Gln245HisfsTer24
ENST00000448076.7:c.1370_1371insTTTTTTTTTTAAT	ENSP00000413452.3:p.Gln457HisfsTer24
ENST00000452863.7:c.1319_1320insTTTTTTTTTTAAT	ENSP00000415516.3:p.Gln440HisfsTer24
ENST00000527882.5:c.351_352insTTTTTTTTTTAAT
ENST00000530998.5:c.683_684insTTTTTTTTTTAAT	ENSP00000435307.1:p.Gln228HisfsTer24
NM_000378.4:c.1319_1320insTTTTTTTTTTAAT	NP_000369.3:p.Gln440HisfsTer24
NM_001198551.1:c.734_735insTTTTTTTTTTAAT , LRG_525t2:c.734_735insTTTTTTTTTTAAT	NP_001185480.1:p.Gln245HisfsTer24
NM_001198552.1:c.683_684insTTTTTTTTTTAAT	NP_001185481.1:p.Gln228HisfsTer24
NM_024424.3:c.1370_1371insTTTTTTTTTTAAT	NP_077742.2:p.Gln457HisfsTer24
NM_024426.4:c.1370_1371insTTTTTTTTTTAAT	NP_077744.3:p.Gln457HisfsTer24
NM_000378.5:c.1334_1335insTTTTTTTTTTAAT	NP_000369.4:p.Gln445HisfsTer24
NM_024424.4:c.1385_1386insTTTTTTTTTTAAT	NP_077742.3:p.Gln462HisfsTer24
NM_024426.5:c.1385_1386insTTTTTTTTTTAAT	NP_077744.4:p.Gln462HisfsTer24
NM_001367854.1:c.197_198insTTTTTTTTTTAAT	NP_001354783.1:p.Gln66HisfsTer24
NR_160306.1:n.1717_1718insTTTTTTTTTTAAT
NM_000378.6:c.1334_1335insTTTTTTTTTTAAT	NP_000369.4:p.Gln445HisfsTer24
NM_001198552.2:c.683_684insTTTTTTTTTTAAT	NP_001185481.1:p.Gln228HisfsTer24
NM_024424.5:c.1385_1386insTTTTTTTTTTAAT	NP_077742.3:p.Gln462HisfsTer24
NM_024426.6:c.1385_1386insTTTTTTTTTTAAT MANE Select	NP_077744.4:p.Gln462HisfsTer24