Canonical Allele Identifier: CA2695201112

Gene: WT1

Linked Data

• ClinVar Variation Id: 2630893
• ClinVar RCV Id: RCV004550668

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434983del , CM000673.2:g.32434983del	GRCh38
NC_000011.9:g.32456529del , CM000673.1:g.32456529del	GRCh37
NC_000011.8:g.32413105del	NCBI36
NG_009272.1:g.5562del , LRG_525:g.5562del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.381del	ENSP00000331327.5:p.Ala128ArgfsTer?
ENST00000379077.9:c.381del	ENSP00000368368.5:p.Ala128ArgfsTer?
ENST00000448076.9:c.381del	ENSP00000413452.5:p.Ala128ArgfsTer?
ENST00000452863.10:c.381del MANE Select	ENSP00000415516.5:p.Ala128ArgfsTer?
ENST00000639563.3:c.381del	ENSP00000492269.3:p.Ala128ArgfsTer?
ENST00000332351.7:c.366del	ENSP00000331327.3:p.Ala123ArgfsTer?
ENST00000379077.7:c.366del	ENSP00000368368.3:p.Ala123ArgfsTer?
ENST00000448076.7:c.366del	ENSP00000413452.3:p.Ala123ArgfsTer?
ENST00000452863.7:c.366del	ENSP00000415516.3:p.Ala123ArgfsTer?
NM_000378.4:c.366del	NP_000369.3:p.Ala123ArgfsTer?
NM_024424.3:c.366del	NP_077742.2:p.Ala123ArgfsTer?
NM_024426.4:c.366del	NP_077744.3:p.Ala123ArgfsTer?
NM_000378.5:c.381del	NP_000369.4:p.Ala128ArgfsTer?
NM_024424.4:c.381del	NP_077742.3:p.Ala128ArgfsTer?
NM_024426.5:c.381del	NP_077744.4:p.Ala128ArgfsTer?
NR_160306.1:n.560del
NM_000378.6:c.381del	NP_000369.4:p.Ala128ArgfsTer?
NM_024424.5:c.381del	NP_077742.3:p.Ala128ArgfsTer?
NM_024426.6:c.381del MANE Select	NP_077744.4:p.Ala128ArgfsTer?