Canonical Allele Identifier: CA645577457

Gene: WT1

Linked Data

• COSMIC: COSM6023016

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392029_32392030insAGAG , CM000673.2:g.32392029_32392030insAGAG	GRCh38
NC_000011.9:g.32413575_32413576insAGAG , CM000673.1:g.32413575_32413576insAGAG	GRCh37
NC_000011.8:g.32370151_32370152insAGAG	NCBI36
NG_009272.1:g.48512_48513insCTCT , LRG_525:g.48512_48513insCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1338_1339insCTCT	ENSP00000331327.5:p.Lys447LeufsTer2
ENST00000379077.9:c.*573_*574insCTCT	ENSP00000368368.5:n.*573_*574insCTCT
ENST00000379079.8:c.738_739insCTCT	ENSP00000368370.2:p.Lys247LeufsTer2
ENST00000448076.9:c.1389_1390insCTCT	ENSP00000413452.5:p.Lys464LeufsTer2
ENST00000452863.10:c.1389_1390insCTCT MANE Select	ENSP00000415516.5:p.Lys464LeufsTer2
ENST00000526685.2:n.843_844insCTCT
ENST00000639563.3:c.1338_1339insCTCT	ENSP00000492269.3:p.Lys447LeufsTer2
ENST00000639907.2:n.532_533insCTCT
ENST00000640146.2:c.714_715insCTCT	ENSP00000491984.2:p.Lys239LeufsTer2
ENST00000650745.1:n.1199_1200insCTCT
ENST00000650861.1:n.1970_1971insCTCT
ENST00000650986.1:n.52_53insCTCT
ENST00000651459.1:c.160_161insCTCT
ENST00000651533.1:n.435_436insCTCT
ENST00000651668.1:n.326_327insCTCT
ENST00000651794.1:n.1232_1233insCTCT
ENST00000651819.1:n.314_315insCTCT
ENST00000652579.1:n.649_650insCTCT
ENST00000652724.1:n.579_580insCTCT
ENST00000332351.7:c.1374_1375insCTCT	ENSP00000331327.3:p.Lys459LeufsTer2
ENST00000379077.7:c.*573_*574insCTCT	ENSP00000368368.3:n.*573_*574insCTCT
ENST00000379079.6:c.738_739insCTCT	ENSP00000368370.2:p.Lys247LeufsTer2
ENST00000448076.7:c.1374_1375insCTCT	ENSP00000413452.3:p.Lys459LeufsTer2
ENST00000452863.7:c.1323_1324insCTCT	ENSP00000415516.3:p.Lys442LeufsTer2
ENST00000527882.5:c.355_356insCTCT
ENST00000530998.5:c.687_688insCTCT	ENSP00000435307.1:p.Lys230LeufsTer2
NM_000378.4:c.1323_1324insCTCT	NP_000369.3:p.Lys442LeufsTer2
NM_001198551.1:c.738_739insCTCT , LRG_525t2:c.738_739insCTCT	NP_001185480.1:p.Lys247LeufsTer2
NM_001198552.1:c.687_688insCTCT	NP_001185481.1:p.Lys230LeufsTer2
NM_024424.3:c.1374_1375insCTCT	NP_077742.2:p.Lys459LeufsTer2
NM_024426.4:c.1374_1375insCTCT	NP_077744.3:p.Lys459LeufsTer2
NM_000378.5:c.1338_1339insCTCT	NP_000369.4:p.Lys447LeufsTer2
NM_024424.4:c.1389_1390insCTCT	NP_077742.3:p.Lys464LeufsTer2
NM_024426.5:c.1389_1390insCTCT	NP_077744.4:p.Lys464LeufsTer2
NM_001367854.1:c.201_202insCTCT	NP_001354783.1:p.Lys68LeufsTer2
NR_160306.1:n.1721_1722insCTCT
NM_000378.6:c.1338_1339insCTCT	NP_000369.4:p.Lys447LeufsTer2
NM_001198552.2:c.687_688insCTCT	NP_001185481.1:p.Lys230LeufsTer2
NM_024424.5:c.1389_1390insCTCT	NP_077742.3:p.Lys464LeufsTer2
NM_024426.6:c.1389_1390insCTCT MANE Select	NP_077744.4:p.Lys464LeufsTer2