Canonical Allele Identifier: CA645577482

Gene: WT1

Linked Data

• COSMIC: COSM1168038

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396258_32396408del , CM000673.2:g.32396258_32396408del	GRCh38
NC_000011.9:g.32417804_32417954del , CM000673.1:g.32417804_32417954del	GRCh37
NC_000011.8:g.32374380_32374530del	NCBI36
NG_009272.1:g.44136_44286del , LRG_525:g.44136_44286del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1064_1213+1del
ENST00000379077.9:c.*299_*448+1del
ENST00000379079.8:c.464_613+1del
ENST00000448076.9:c.1115_1264+1del
ENST00000452863.10:c.1115_1264+1del
ENST00000526685.2:n.569_718+1del
ENST00000639563.3:c.1064_1213+1del
ENST00000639907.2:n.258_407+1del
ENST00000640146.2:c.440_589+1del
ENST00000650861.1:n.1696_1845+1del
ENST00000651459.1:c.35+3542_36-3501del
ENST00000651668.1:n.52_201+1del
ENST00000651794.1:n.858_1008del
ENST00000651819.1:n.40_189+1del
ENST00000652579.1:n.275_425del
ENST00000652724.1:n.305_454+1del
ENST00000332351.7:c.1100_1249+1del
ENST00000379077.7:c.*299_*448+1del
ENST00000379079.6:c.464_613+1del
ENST00000448076.7:c.1100_1249+1del
ENST00000452863.7:c.1049_1198+1del
ENST00000527882.5:c.171_320+1del
ENST00000530998.5:c.413_562+1del
NM_000378.4:c.1049_1198+1del
NM_001198551.1:c.464_613+1del , LRG_525t2:c.464_613+1del
NM_001198552.1:c.413_562+1del
NM_024424.3:c.1100_1249+1del
NM_024426.4:c.1100_1249+1del
NM_000378.5:c.1064_1213+1del
NM_024424.4:c.1115_1264+1del
NM_024426.5:c.1115_1264+1del
NM_001367854.1:c.-74_76+1del
NR_160306.1:n.1447_1596+1del
NM_000378.6:c.1064_1213+1del
NM_001198552.2:c.413_562+1del
NM_024424.5:c.1115_1264+1del
NM_024426.6:c.1115_1264+1del