Canonical Allele Identifier: CA2695213676

Gene: WT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434934_32434946dup , CM000673.2:g.32434934_32434946dup	GRCh38
NC_000011.9:g.32456480_32456492dup , CM000673.1:g.32456480_32456492dup	GRCh37
NC_000011.8:g.32413056_32413068dup	NCBI36
NG_009272.1:g.5598_5610dup , LRG_525:g.5598_5610dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.417_429dup	ENSP00000331327.5:p.Phe144AlafsTer?
ENST00000379077.9:c.417_429dup	ENSP00000368368.5:p.Phe144AlafsTer?
ENST00000448076.9:c.417_429dup	ENSP00000413452.5:p.Phe144AlafsTer?
ENST00000452863.10:c.417_429dup MANE Select	ENSP00000415516.5:p.Phe144AlafsTer?
ENST00000639563.3:c.417_429dup	ENSP00000492269.3:p.Phe144AlafsTer?
ENST00000332351.7:c.402_414dup	ENSP00000331327.3:p.Phe139AlafsTer?
ENST00000379077.7:c.402_414dup	ENSP00000368368.3:p.Phe139AlafsTer?
ENST00000448076.7:c.402_414dup	ENSP00000413452.3:p.Phe139AlafsTer?
ENST00000452863.7:c.402_414dup	ENSP00000415516.3:p.Phe139AlafsTer?
NM_000378.4:c.402_414dup	NP_000369.3:p.Phe139AlafsTer?
NM_024424.3:c.402_414dup	NP_077742.2:p.Phe139AlafsTer?
NM_024426.4:c.402_414dup	NP_077744.3:p.Phe139AlafsTer?
NM_000378.5:c.417_429dup	NP_000369.4:p.Phe144AlafsTer?
NM_024424.4:c.417_429dup	NP_077742.3:p.Phe144AlafsTer?
NM_024426.5:c.417_429dup	NP_077744.4:p.Phe144AlafsTer?
NR_160306.1:n.596_608dup
NM_000378.6:c.417_429dup	NP_000369.4:p.Phe144AlafsTer?
NM_024424.5:c.417_429dup	NP_077742.3:p.Phe144AlafsTer?
NM_024426.6:c.417_429dup MANE Select	NP_077744.4:p.Phe144AlafsTer?