Canonical Allele Identifier: CA2574790569

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435255del , CM000673.2:g.32435255del	GRCh38
NC_000011.9:g.32456801del , CM000673.1:g.32456801del	GRCh37
NC_000011.8:g.32413377del	NCBI36
NG_009272.1:g.5287del , LRG_525:g.5287del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.106del	ENSP00000331327.5:p.Gln36ArgfsTer13
ENST00000379077.9:c.106del	ENSP00000368368.5:p.Gln36ArgfsTer13
ENST00000448076.9:c.106del	ENSP00000413452.5:p.Gln36ArgfsTer13
ENST00000452863.10:c.106del MANE Select	ENSP00000415516.5:p.Gln36ArgfsTer13
ENST00000639563.3:c.106del	ENSP00000492269.3:p.Gln36ArgfsTer13
ENST00000332351.7:c.91del	ENSP00000331327.3:p.Gln31ArgfsTer13
ENST00000379077.7:c.91del	ENSP00000368368.3:p.Gln31ArgfsTer13
ENST00000448076.7:c.91del	ENSP00000413452.3:p.Gln31ArgfsTer13
ENST00000452863.7:c.91del	ENSP00000415516.3:p.Gln31ArgfsTer13
NM_000378.4:c.91del	NP_000369.3:p.Gln31ArgfsTer13
NM_024424.3:c.91del	NP_077742.2:p.Gln31ArgfsTer13
NM_024426.4:c.91del	NP_077744.3:p.Gln31ArgfsTer13
NM_000378.5:c.106del	NP_000369.4:p.Gln36ArgfsTer13
NM_024424.4:c.106del	NP_077742.3:p.Gln36ArgfsTer13
NM_024426.5:c.106del	NP_077744.4:p.Gln36ArgfsTer13
NR_160306.1:n.285del
NM_000378.6:c.106del	NP_000369.4:p.Gln36ArgfsTer13
NM_024424.5:c.106del	NP_077742.3:p.Gln36ArgfsTer13
NM_024426.6:c.106del MANE Select	NP_077744.4:p.Gln36ArgfsTer13