Canonical Allele Identifier: CA645577488

Gene: WT1

Linked Data

• COSMIC: COSM1317329 ; COSM1317330

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396302_32396303del , CM000673.2:g.32396302_32396303del	GRCh38
NC_000011.9:g.32417848_32417849del , CM000673.1:g.32417848_32417849del	GRCh37
NC_000011.8:g.32374424_32374425del	NCBI36
NG_009272.1:g.44241_44242del , LRG_525:g.44241_44242del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1169_1170del	ENSP00000331327.5:p.Tyr390PhefsTer2
ENST00000379077.9:c.*404_*405del	ENSP00000368368.5:n.*404_*405del
ENST00000379079.8:c.569_570del	ENSP00000368370.2:p.Tyr190PhefsTer2
ENST00000448076.9:c.1220_1221del	ENSP00000413452.5:p.Tyr407PhefsTer2
ENST00000452863.10:c.1220_1221del MANE Select	ENSP00000415516.5:p.Tyr407PhefsTer2
ENST00000526685.2:n.674_675del
ENST00000639563.3:c.1169_1170del	ENSP00000492269.3:p.Tyr390PhefsTer2
ENST00000639907.2:n.363_364del
ENST00000640146.2:c.545_546del	ENSP00000491984.2:p.Tyr182PhefsTer2
ENST00000650861.1:n.1801_1802del
ENST00000651459.1:c.36-3546_36-3545del
ENST00000651668.1:n.157_158del
ENST00000651794.1:n.963_964del
ENST00000651819.1:n.145_146del
ENST00000652579.1:n.380_381del
ENST00000652724.1:n.410_411del
ENST00000332351.7:c.1205_1206del	ENSP00000331327.3:p.Tyr402PhefsTer2
ENST00000379077.7:c.*404_*405del	ENSP00000368368.3:n.*404_*405del
ENST00000379079.6:c.569_570del	ENSP00000368370.2:p.Tyr190PhefsTer2
ENST00000448076.7:c.1205_1206del	ENSP00000413452.3:p.Tyr402PhefsTer2
ENST00000452863.7:c.1154_1155del	ENSP00000415516.3:p.Tyr385PhefsTer2
ENST00000526685.1:c.32_33del	ENSP00000436292.1:p.Tyr11PhefsTer2
ENST00000527882.5:c.276_277del
ENST00000530998.5:c.518_519del	ENSP00000435307.1:p.Tyr173PhefsTer2
NM_000378.4:c.1154_1155del	NP_000369.3:p.Tyr385PhefsTer2
NM_001198551.1:c.569_570del , LRG_525t2:c.569_570del	NP_001185480.1:p.Tyr190PhefsTer2
NM_001198552.1:c.518_519del	NP_001185481.1:p.Tyr173PhefsTer2
NM_024424.3:c.1205_1206del	NP_077742.2:p.Tyr402PhefsTer2
NM_024426.4:c.1205_1206del	NP_077744.3:p.Tyr402PhefsTer2
NM_000378.5:c.1169_1170del	NP_000369.4:p.Tyr390PhefsTer2
NM_024424.4:c.1220_1221del	NP_077742.3:p.Tyr407PhefsTer2
NM_024426.5:c.1220_1221del	NP_077744.4:p.Tyr407PhefsTer2
NM_001367854.1:c.32_33del	NP_001354783.1:p.Tyr11PhefsTer2
NR_160306.1:n.1552_1553del
NM_000378.6:c.1169_1170del	NP_000369.4:p.Tyr390PhefsTer2
NM_001198552.2:c.518_519del	NP_001185481.1:p.Tyr173PhefsTer2
NM_024424.5:c.1220_1221del	NP_077742.3:p.Tyr407PhefsTer2
NM_024426.6:c.1220_1221del MANE Select	NP_077744.4:p.Tyr407PhefsTer2