Canonical Allele Identifier: CA2612989400

Gene: WT1

Linked Data

• gnomAD v4: 11-32434844-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434844_32434845insGG , CM000673.2:g.32434844_32434845insGG	GRCh38
NC_000011.9:g.32456390_32456391insGG , CM000673.1:g.32456390_32456391insGG	GRCh37
NC_000011.8:g.32412966_32412967insGG	NCBI36
NG_009272.1:g.5697_5698insCC , LRG_525:g.5697_5698insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.516_517insCC	ENSP00000331327.5:p.Phe173ProfsTer?
ENST00000379077.9:c.516_517insCC	ENSP00000368368.5:p.Phe173ProfsTer?
ENST00000448076.9:c.516_517insCC	ENSP00000413452.5:p.Phe173ProfsTer?
ENST00000452863.10:c.516_517insCC MANE Select	ENSP00000415516.5:p.Phe173ProfsTer?
ENST00000639563.3:c.516_517insCC	ENSP00000492269.3:p.Phe173ProfsTer?
ENST00000332351.7:c.501_502insCC	ENSP00000331327.3:p.Phe168ProfsTer?
ENST00000379077.7:c.501_502insCC	ENSP00000368368.3:p.Phe168ProfsTer?
ENST00000448076.7:c.501_502insCC	ENSP00000413452.3:p.Phe168ProfsTer?
ENST00000452863.7:c.501_502insCC	ENSP00000415516.3:p.Phe168ProfsTer?
NM_000378.4:c.501_502insCC	NP_000369.3:p.Phe168ProfsTer?
NM_024424.3:c.501_502insCC	NP_077742.2:p.Phe168ProfsTer?
NM_024426.4:c.501_502insCC	NP_077744.3:p.Phe168ProfsTer?
NM_000378.5:c.516_517insCC	NP_000369.4:p.Phe173ProfsTer?
NM_024424.4:c.516_517insCC	NP_077742.3:p.Phe173ProfsTer?
NM_024426.5:c.516_517insCC	NP_077744.4:p.Phe173ProfsTer?
NR_160306.1:n.695_696insCC
NM_000378.6:c.516_517insCC	NP_000369.4:p.Phe173ProfsTer?
NM_024424.5:c.516_517insCC	NP_077742.3:p.Phe173ProfsTer?
NM_024426.6:c.516_517insCC MANE Select	NP_077744.4:p.Phe173ProfsTer?