Canonical Allele Identifier: CA2612989682

Gene: WT1

Linked Data

• gnomAD v4: 11-32435301-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435302_32435303dup , CM000673.2:g.32435302_32435303dup	GRCh38
NC_000011.9:g.32456848_32456849dup , CM000673.1:g.32456848_32456849dup	GRCh37
NC_000011.8:g.32413424_32413425dup	NCBI36
NG_009272.1:g.5239_5240dup , LRG_525:g.5239_5240dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.58_59dup	ENSP00000331327.5:p.Gln20HisfsTer30
ENST00000379077.9:c.58_59dup	ENSP00000368368.5:p.Gln20HisfsTer30
ENST00000448076.9:c.58_59dup	ENSP00000413452.5:p.Gln20HisfsTer30
ENST00000452863.10:c.58_59dup MANE Select	ENSP00000415516.5:p.Gln20HisfsTer30
ENST00000639563.3:c.58_59dup	ENSP00000492269.3:p.Gln20HisfsTer30
ENST00000332351.7:c.43_44dup	ENSP00000331327.3:p.Gln15HisfsTer30
ENST00000379077.7:c.43_44dup	ENSP00000368368.3:p.Gln15HisfsTer30
ENST00000448076.7:c.43_44dup	ENSP00000413452.3:p.Gln15HisfsTer30
ENST00000452863.7:c.43_44dup	ENSP00000415516.3:p.Gln15HisfsTer30
NM_000378.4:c.43_44dup	NP_000369.3:p.Gln15HisfsTer30
NM_024424.3:c.43_44dup	NP_077742.2:p.Gln15HisfsTer30
NM_024426.4:c.43_44dup	NP_077744.3:p.Gln15HisfsTer30
NM_000378.5:c.58_59dup	NP_000369.4:p.Gln20HisfsTer30
NM_024424.4:c.58_59dup	NP_077742.3:p.Gln20HisfsTer30
NM_024426.5:c.58_59dup	NP_077744.4:p.Gln20HisfsTer30
NR_160306.1:n.237_238dup
NM_000378.6:c.58_59dup	NP_000369.4:p.Gln20HisfsTer30
NM_024424.5:c.58_59dup	NP_077742.3:p.Gln20HisfsTer30
NM_024426.6:c.58_59dup MANE Select	NP_077744.4:p.Gln20HisfsTer30