Canonical Allele Identifier: CA645577450

Gene: WT1

Linked Data

• COSMIC: COSM144850

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32392023_32392028del , CM000673.2:g.32392023_32392028del	GRCh38
NC_000011.9:g.32413569_32413574del , CM000673.1:g.32413569_32413574del	GRCh37
NC_000011.8:g.32370145_32370150del	NCBI36
NG_009272.1:g.48514_48519del , LRG_525:g.48514_48519del

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.1340_1345del	ENSP00000331327.5:p.Lys447_Ser449delinsThr
ENST00000379077.9:c.*575_*580del	ENSP00000368368.5:n.*575_*580del
ENST00000379079.8:c.740_745del	ENSP00000368370.2:p.Lys247_Ser249delinsThr
ENST00000448076.9:c.1391_1396del	ENSP00000413452.5:p.Lys464_Ser466delinsThr
ENST00000452863.10:c.1391_1396del MANE Select	ENSP00000415516.5:p.Lys464_Ser466delinsThr
ENST00000526685.2:n.845_850del
ENST00000639563.3:c.1340_1345del	ENSP00000492269.3:p.Lys447_Ser449delinsThr
ENST00000639907.2:n.534_539del
ENST00000640146.2:c.716_721del	ENSP00000491984.2:p.Lys239_Ser241delinsThr
ENST00000650745.1:n.1201_1206del
ENST00000650861.1:n.1972_1977del
ENST00000650986.1:n.54_59del
ENST00000651459.1:c.162_167del
ENST00000651533.1:n.437_442del
ENST00000651668.1:n.328_333del
ENST00000651794.1:n.1234_1239del
ENST00000651819.1:n.316_321del
ENST00000652579.1:n.651_656del
ENST00000652724.1:n.581_586del
ENST00000332351.7:c.1376_1381del	ENSP00000331327.3:p.Lys459_Ser461delinsThr
ENST00000379077.7:c.*575_*580del	ENSP00000368368.3:n.*575_*580del
ENST00000379079.6:c.740_745del	ENSP00000368370.2:p.Lys247_Ser249delinsThr
ENST00000448076.7:c.1376_1381del	ENSP00000413452.3:p.Lys459_Ser461delinsThr
ENST00000452863.7:c.1325_1330del	ENSP00000415516.3:p.Lys442_Ser444delinsThr
ENST00000527882.5:c.357_362del
ENST00000530998.5:c.689_694del	ENSP00000435307.1:p.Lys230_Ser232delinsThr
NM_000378.4:c.1325_1330del	NP_000369.3:p.Lys442_Ser444delinsThr
NM_001198551.1:c.740_745del , LRG_525t2:c.740_745del	NP_001185480.1:p.Lys247_Ser249delinsThr
NM_001198552.1:c.689_694del	NP_001185481.1:p.Lys230_Ser232delinsThr
NM_024424.3:c.1376_1381del	NP_077742.2:p.Lys459_Ser461delinsThr
NM_024426.4:c.1376_1381del	NP_077744.3:p.Lys459_Ser461delinsThr
NM_000378.5:c.1340_1345del	NP_000369.4:p.Lys447_Ser449delinsThr
NM_024424.4:c.1391_1396del	NP_077742.3:p.Lys464_Ser466delinsThr
NM_024426.5:c.1391_1396del	NP_077744.4:p.Lys464_Ser466delinsThr
NM_001367854.1:c.203_208del	NP_001354783.1:p.Lys68_Ser70delinsThr
NR_160306.1:n.1723_1728del
NM_000378.6:c.1340_1345del	NP_000369.4:p.Lys447_Ser449delinsThr
NM_001198552.2:c.689_694del	NP_001185481.1:p.Lys230_Ser232delinsThr
NM_024424.5:c.1391_1396del	NP_077742.3:p.Lys464_Ser466delinsThr
NM_024426.6:c.1391_1396del MANE Select	NP_077744.4:p.Lys464_Ser466delinsThr