Canonical Allele Identifier: CA2695213674
Gene: WT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32434862_32434863del , CM000673.2:g.32434862_32434863del GRCh38
NC_000011.9:g.32456408_32456409del , CM000673.1:g.32456408_32456409del GRCh37
NC_000011.8:g.32412984_32412985del NCBI36
NG_009272.1:g.5680_5681del , LRG_525:g.5680_5681del

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.499_500del ENSP00000331327.5:p.Val167ProfsTer?
ENST00000379077.9:c.499_500del ENSP00000368368.5:p.Val167ProfsTer?
ENST00000448076.9:c.499_500del ENSP00000413452.5:p.Val167ProfsTer?
ENST00000452863.10:c.499_500del MANE Select ENSP00000415516.5:p.Val167ProfsTer?
ENST00000639563.3:c.499_500del ENSP00000492269.3:p.Val167ProfsTer?
ENST00000332351.7:c.484_485del ENSP00000331327.3:p.Val162ProfsTer?
ENST00000379077.7:c.484_485del ENSP00000368368.3:p.Val162ProfsTer?
ENST00000448076.7:c.484_485del ENSP00000413452.3:p.Val162ProfsTer?
ENST00000452863.7:c.484_485del ENSP00000415516.3:p.Val162ProfsTer?
NM_000378.4:c.484_485del NP_000369.3:p.Val162ProfsTer?
NM_024424.3:c.484_485del NP_077742.2:p.Val162ProfsTer?
NM_024426.4:c.484_485del NP_077744.3:p.Val162ProfsTer?
NM_000378.5:c.499_500del NP_000369.4:p.Val167ProfsTer?
NM_024424.4:c.499_500del NP_077742.3:p.Val167ProfsTer?
NM_024426.5:c.499_500del NP_077744.4:p.Val167ProfsTer?
NR_160306.1:n.678_679del
NM_000378.6:c.499_500del NP_000369.4:p.Val167ProfsTer?
NM_024424.5:c.499_500del NP_077742.3:p.Val167ProfsTer?
NM_024426.6:c.499_500del MANE Select NP_077744.4:p.Val167ProfsTer?