Canonical Allele Identifier: CA2580084154

Gene: WT1

Linked Data

• ClinVar Variation Id: 1696388
• ClinVar RCV Id: RCV002266533
• dbSNP Id: rs2133102575

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434848del , CM000673.2:g.32434848del	GRCh38
NC_000011.9:g.32456394del , CM000673.1:g.32456394del	GRCh37
NC_000011.8:g.32412970del	NCBI36
NG_009272.1:g.5695del , LRG_525:g.5695del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.514del	ENSP00000331327.5:p.Gln172SerfsTer?
ENST00000379077.9:c.514del	ENSP00000368368.5:p.Gln172SerfsTer?
ENST00000448076.9:c.514del	ENSP00000413452.5:p.Gln172SerfsTer?
ENST00000452863.10:c.514del MANE Select	ENSP00000415516.5:p.Gln172SerfsTer?
ENST00000639563.3:c.514del	ENSP00000492269.3:p.Gln172SerfsTer?
ENST00000332351.7:c.499del	ENSP00000331327.3:p.Gln167SerfsTer?
ENST00000379077.7:c.499del	ENSP00000368368.3:p.Gln167SerfsTer?
ENST00000448076.7:c.499del	ENSP00000413452.3:p.Gln167SerfsTer?
ENST00000452863.7:c.499del	ENSP00000415516.3:p.Gln167SerfsTer?
NM_000378.4:c.499del	NP_000369.3:p.Gln167SerfsTer?
NM_024424.3:c.499del	NP_077742.2:p.Gln167SerfsTer?
NM_024426.4:c.499del	NP_077744.3:p.Gln167SerfsTer?
NM_000378.5:c.514del	NP_000369.4:p.Gln172SerfsTer?
NM_024424.4:c.514del	NP_077742.3:p.Gln172SerfsTer?
NM_024426.5:c.514del	NP_077744.4:p.Gln172SerfsTer?
NR_160306.1:n.693del
NM_000378.6:c.514del	NP_000369.4:p.Gln172SerfsTer?
NM_024424.5:c.514del	NP_077742.3:p.Gln172SerfsTer?
NM_024426.6:c.514del MANE Select	NP_077744.4:p.Gln172SerfsTer?