Canonical Allele Identifier: CA473773685

Gene: WT1

Linked Data

• COSMIC: COSM27369
• MyVariant Identifiers: chr11:g.32456516del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434970del , CM000673.2:g.32434970del	GRCh38
NC_000011.9:g.32456516del , CM000673.1:g.32456516del	GRCh37
NC_000011.8:g.32413092del	NCBI36
NG_009272.1:g.5573del , LRG_525:g.5573del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.392del	ENSP00000331327.5:p.Pro131ArgfsTer?
ENST00000379077.9:c.392del	ENSP00000368368.5:p.Pro131ArgfsTer?
ENST00000448076.9:c.392del	ENSP00000413452.5:p.Pro131ArgfsTer?
ENST00000452863.10:c.392del MANE Select	ENSP00000415516.5:p.Pro131ArgfsTer?
ENST00000639563.3:c.392del	ENSP00000492269.3:p.Pro131ArgfsTer?
ENST00000332351.7:c.377del	ENSP00000331327.3:p.Pro126ArgfsTer?
ENST00000379077.7:c.377del	ENSP00000368368.3:p.Pro126ArgfsTer?
ENST00000448076.7:c.377del	ENSP00000413452.3:p.Pro126ArgfsTer?
ENST00000452863.7:c.377del	ENSP00000415516.3:p.Pro126ArgfsTer?
NM_000378.4:c.377del	NP_000369.3:p.Pro126ArgfsTer?
NM_024424.3:c.377del	NP_077742.2:p.Pro126ArgfsTer?
NM_024426.4:c.377del	NP_077744.3:p.Pro126ArgfsTer?
NM_000378.5:c.392del	NP_000369.4:p.Pro131ArgfsTer?
NM_024424.4:c.392del	NP_077742.3:p.Pro131ArgfsTer?
NM_024426.5:c.392del	NP_077744.4:p.Pro131ArgfsTer?
NR_160306.1:n.571del
NM_000378.6:c.392del	NP_000369.4:p.Pro131ArgfsTer?
NM_024424.5:c.392del	NP_077742.3:p.Pro131ArgfsTer?
NM_024426.6:c.392del MANE Select	NP_077744.4:p.Pro131ArgfsTer?