Canonical Allele Identifier: CA2573146210

Gene: WT1

Linked Data

• ClinVar Variation Id: 1524014
• ClinVar RCV Id: RCV002031406
• dbSNP Id: rs2133106545

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435196_32435197delinsCA , CM000673.2:g.32435196_32435197delinsCA	GRCh38
NC_000011.9:g.32456742_32456743delinsCA , CM000673.1:g.32456742_32456743delinsCA	GRCh37
NC_000011.8:g.32413318_32413319delinsCA	NCBI36
NG_009272.1:g.5345_5346delinsTG , LRG_525:g.5345_5346delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.164_165delinsTG	ENSP00000331327.5:p.Ala55Val
ENST00000379077.9:c.164_165delinsTG	ENSP00000368368.5:p.Ala55Val
ENST00000448076.9:c.164_165delinsTG	ENSP00000413452.5:p.Ala55Val
ENST00000452863.10:c.164_165delinsTG MANE Select	ENSP00000415516.5:p.Ala55Val
ENST00000639563.3:c.164_165delinsTG	ENSP00000492269.3:p.Ala55Val
ENST00000332351.7:c.149_150delinsTG	ENSP00000331327.3:p.Ala50Val
ENST00000379077.7:c.149_150delinsTG	ENSP00000368368.3:p.Ala50Val
ENST00000448076.7:c.149_150delinsTG	ENSP00000413452.3:p.Ala50Val
ENST00000452863.7:c.149_150delinsTG	ENSP00000415516.3:p.Ala50Val
NM_000378.4:c.149_150delinsTG	NP_000369.3:p.Ala50Val
NM_024424.3:c.149_150delinsTG	NP_077742.2:p.Ala50Val
NM_024426.4:c.149_150delinsTG	NP_077744.3:p.Ala50Val
NM_000378.5:c.164_165delinsTG	NP_000369.4:p.Ala55Val
NM_024424.4:c.164_165delinsTG	NP_077742.3:p.Ala55Val
NM_024426.5:c.164_165delinsTG	NP_077744.4:p.Ala55Val
NR_160306.1:n.343_344delinsTG
NM_000378.6:c.164_165delinsTG	NP_000369.4:p.Ala55Val
NM_024424.5:c.164_165delinsTG	NP_077742.3:p.Ala55Val
NM_024426.6:c.164_165delinsTG MANE Select	NP_077744.4:p.Ala55Val