Canonical Allele Identifier: CA2825001879

Gene: WT1

Linked Data

• ClinVar Variation Id: 3075561
• ClinVar RCV Id: RCV004017079

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435291_32435292del , CM000673.2:g.32435291_32435292del	GRCh38
NC_000011.9:g.32456837_32456838del , CM000673.1:g.32456837_32456838del	GRCh37
NC_000011.8:g.32413413_32413414del	NCBI36
NG_009272.1:g.5250_5251del , LRG_525:g.5250_5251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.69_70del	ENSP00000331327.5:p.Arg24LeufsTer?
ENST00000379077.9:c.69_70del	ENSP00000368368.5:p.Arg24LeufsTer?
ENST00000448076.9:c.69_70del	ENSP00000413452.5:p.Arg24LeufsTer?
ENST00000452863.10:c.69_70del MANE Select	ENSP00000415516.5:p.Arg24LeufsTer?
ENST00000639563.3:c.69_70del	ENSP00000492269.3:p.Arg24LeufsTer?
ENST00000332351.7:c.54_55del	ENSP00000331327.3:p.Arg19LeufsTer?
ENST00000379077.7:c.54_55del	ENSP00000368368.3:p.Arg19LeufsTer?
ENST00000448076.7:c.54_55del	ENSP00000413452.3:p.Arg19LeufsTer?
ENST00000452863.7:c.54_55del	ENSP00000415516.3:p.Arg19LeufsTer?
NM_000378.4:c.54_55del	NP_000369.3:p.Arg19LeufsTer?
NM_024424.3:c.54_55del	NP_077742.2:p.Arg19LeufsTer?
NM_024426.4:c.54_55del	NP_077744.3:p.Arg19LeufsTer?
NM_000378.5:c.69_70del	NP_000369.4:p.Arg24LeufsTer?
NM_024424.4:c.69_70del	NP_077742.3:p.Arg24LeufsTer?
NM_024426.5:c.69_70del	NP_077744.4:p.Arg24LeufsTer?
NR_160306.1:n.248_249del
NM_000378.6:c.69_70del	NP_000369.4:p.Arg24LeufsTer?
NM_024424.5:c.69_70del	NP_077742.3:p.Arg24LeufsTer?
NM_024426.6:c.69_70del MANE Select	NP_077744.4:p.Arg24LeufsTer?