Canonical Allele Identifier: CA645577465

Gene: WT1

Linked Data

• COSMIC: COSM5879203 ; COSM5879204 ; COSM5879205

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392684_32392698del , CM000673.2:g.32392684_32392698del	GRCh38
NC_000011.9:g.32414230_32414244del , CM000673.1:g.32414230_32414244del	GRCh37
NC_000011.8:g.32370806_32370820del	NCBI36
NG_009272.1:g.47848_47862del , LRG_525:g.47848_47862del

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1275_1289del	ENSP00000331327.5:p.Leu426_Gln430del
ENST00000379077.9:c.*510_*524del	ENSP00000368368.5:n.*510_*524del
ENST00000379079.8:c.675_689del	ENSP00000368370.2:p.Leu226_Gln230del
ENST00000448076.9:c.1326_1340del	ENSP00000413452.5:p.Leu443_Gln447del
ENST00000452863.10:c.1326_1340del MANE Select	ENSP00000415516.5:p.Leu443_Gln447del
ENST00000526685.2:n.780_794del
ENST00000639563.3:c.1275_1289del	ENSP00000492269.3:p.Leu426_Gln430del
ENST00000639907.2:n.469_483del
ENST00000640146.2:c.651_665del	ENSP00000491984.2:p.Leu218_Gln222del
ENST00000650745.1:n.535_549del
ENST00000650861.1:n.1907_1921del
ENST00000651459.1:c.97_111del
ENST00000651533.1:n.372_386del
ENST00000651668.1:n.263_277del
ENST00000651794.1:n.1169_1183del
ENST00000651819.1:n.251_265del
ENST00000652579.1:n.586_600del
ENST00000652724.1:n.516_530del
ENST00000332351.7:c.1311_1325del	ENSP00000331327.3:p.Leu438_Gln442del
ENST00000379077.7:c.*510_*524del	ENSP00000368368.3:n.*510_*524del
ENST00000379079.6:c.675_689del	ENSP00000368370.2:p.Leu226_Gln230del
ENST00000448076.7:c.1311_1325del	ENSP00000413452.3:p.Leu438_Gln442del
ENST00000452863.7:c.1260_1274del	ENSP00000415516.3:p.Leu421_Gln425del
ENST00000527882.5:c.321-630_321-616del
ENST00000530998.5:c.624_638del	ENSP00000435307.1:p.Leu209_Gln213del
NM_000378.4:c.1260_1274del	NP_000369.3:p.Leu421_Gln425del
NM_001198551.1:c.675_689del , LRG_525t2:c.675_689del	NP_001185480.1:p.Leu226_Gln230del
NM_001198552.1:c.624_638del	NP_001185481.1:p.Leu209_Gln213del
NM_024424.3:c.1311_1325del	NP_077742.2:p.Leu438_Gln442del
NM_024426.4:c.1311_1325del	NP_077744.3:p.Leu438_Gln442del
NM_000378.5:c.1275_1289del	NP_000369.4:p.Leu426_Gln430del
NM_024424.4:c.1326_1340del	NP_077742.3:p.Leu443_Gln447del
NM_024426.5:c.1326_1340del	NP_077744.4:p.Leu443_Gln447del
NM_001367854.1:c.138_152del	NP_001354783.1:p.Leu47_Gln51del
NR_160306.1:n.1658_1672del
NM_000378.6:c.1275_1289del	NP_000369.4:p.Leu426_Gln430del
NM_001198552.2:c.624_638del	NP_001185481.1:p.Leu209_Gln213del
NM_024424.5:c.1326_1340del	NP_077742.3:p.Leu443_Gln447del
NM_024426.6:c.1326_1340del MANE Select	NP_077744.4:p.Leu443_Gln447del