Canonical Allele Identifier: CA645577563

Gene: WT1

Linked Data

• COSMIC: COSM28948 ; COSM4775079 ; COSM4775080

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32396367_32396368insT , CM000673.2:g.32396367_32396368insT	GRCh38
NC_000011.9:g.32417913_32417914insT , CM000673.1:g.32417913_32417914insT	GRCh37
NC_000011.8:g.32374489_32374490insT	NCBI36
NG_009272.1:g.44174_44175insA , LRG_525:g.44174_44175insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.1102_1103insA	ENSP00000331327.5:p.Arg368GlnfsTer5
ENST00000379077.9:c.*337_*338insA	ENSP00000368368.5:n.*337_*338insA
ENST00000379079.8:c.502_503insA	ENSP00000368370.2:p.Arg168GlnfsTer5
ENST00000448076.9:c.1153_1154insA	ENSP00000413452.5:p.Arg385GlnfsTer5
ENST00000452863.10:c.1153_1154insA MANE Select	ENSP00000415516.5:p.Arg385GlnfsTer5
ENST00000526685.2:n.607_608insA
ENST00000639563.3:c.1102_1103insA	ENSP00000492269.3:p.Arg368GlnfsTer5
ENST00000639907.2:n.296_297insA
ENST00000640146.2:c.478_479insA	ENSP00000491984.2:p.Arg160GlnfsTer5
ENST00000650861.1:n.1734_1735insA
ENST00000651459.1:c.35+3580_35+3581insA
ENST00000651668.1:n.90_91insA
ENST00000651794.1:n.896_897insA
ENST00000651819.1:n.78_79insA
ENST00000652579.1:n.313_314insA
ENST00000652724.1:n.343_344insA
ENST00000332351.7:c.1138_1139insA	ENSP00000331327.3:p.Arg380GlnfsTer5
ENST00000379077.7:c.*337_*338insA	ENSP00000368368.3:n.*337_*338insA
ENST00000379079.6:c.502_503insA	ENSP00000368370.2:p.Arg168GlnfsTer5
ENST00000448076.7:c.1138_1139insA	ENSP00000413452.3:p.Arg380GlnfsTer5
ENST00000452863.7:c.1087_1088insA	ENSP00000415516.3:p.Arg363GlnfsTer5
ENST00000526685.1:c.-36_-35insA	ENSP00000436292.1:n.-36_-35insA
ENST00000527775.1:c.391_392insA	ENSP00000435351.1:p.Arg131GlnfsTer?
ENST00000527882.5:c.209_210insA
ENST00000530998.5:c.451_452insA	ENSP00000435307.1:p.Arg151GlnfsTer5
NM_000378.4:c.1087_1088insA	NP_000369.3:p.Arg363GlnfsTer5
NM_001198551.1:c.502_503insA , LRG_525t2:c.502_503insA	NP_001185480.1:p.Arg168GlnfsTer5
NM_001198552.1:c.451_452insA	NP_001185481.1:p.Arg151GlnfsTer5
NM_024424.3:c.1138_1139insA	NP_077742.2:p.Arg380GlnfsTer5
NM_024426.4:c.1138_1139insA	NP_077744.3:p.Arg380GlnfsTer5
NM_000378.5:c.1102_1103insA	NP_000369.4:p.Arg368GlnfsTer5
NM_024424.4:c.1153_1154insA	NP_077742.3:p.Arg385GlnfsTer5
NM_024426.5:c.1153_1154insA	NP_077744.4:p.Arg385GlnfsTer5
NM_001367854.1:c.-36_-35insA	NP_001354783.1:n.-36_-35insA
NR_160306.1:n.1485_1486insA
NM_000378.6:c.1102_1103insA	NP_000369.4:p.Arg368GlnfsTer5
NM_001198552.2:c.451_452insA	NP_001185481.1:p.Arg151GlnfsTer5
NM_024424.5:c.1153_1154insA	NP_077742.3:p.Arg385GlnfsTer5
NM_024426.6:c.1153_1154insA MANE Select	NP_077744.4:p.Arg385GlnfsTer5