Canonical Allele Identifier: CA645577714

Gene: WT1

Linked Data

• COSMIC: COSM250067

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32428498_32428620del , CM000673.2:g.32428498_32428620del	GRCh38
NC_000011.9:g.32450044_32450166del , CM000673.1:g.32450044_32450166del	GRCh37
NC_000011.8:g.32406620_32406742del	NCBI36
NG_009272.1:g.11925_12047del , LRG_525:g.11925_12047del

Transcript Alleles

HGVS	Amino-acid change
ENST00000332351.9:c.664_784+2del
ENST00000379077.9:c.664_784+2del
ENST00000379079.8:c.13_133+2del
ENST00000448076.9:c.664_784+2del
ENST00000452863.10:c.664_784+2del
ENST00000639563.3:c.664_784+2del
ENST00000640146.2:c.40_160+2del
ENST00000332351.7:c.649_769+2del
ENST00000379077.7:c.649_769+2del
ENST00000379079.6:c.13_133+2del
ENST00000448076.7:c.649_769+2del
ENST00000452863.7:c.649_769+2del
ENST00000527775.1:c.-99_22+2del
ENST00000530998.5:c.13_133+2del
NM_000378.4:c.649_769+2del
NM_001198551.1:c.13_133+2del , LRG_525t2:c.13_133+2del
NM_001198552.1:c.13_133+2del
NM_024424.3:c.649_769+2del
NM_024426.4:c.649_769+2del
NM_000378.5:c.664_784+2del
NM_024424.4:c.664_784+2del
NM_024426.5:c.664_784+2del
NR_160306.1:n.843_963+2del
NM_000378.6:c.664_784+2del
NM_001198552.2:c.13_133+2del
NM_024424.5:c.664_784+2del
NM_024426.6:c.664_784+2del