Canonical Allele Identifier: CA598513625

Gene: WT1

Linked Data

• dbSNP Id: rs1357873392
• gnomAD v2: 11-32456455-CAGCT-C
• gnomAD v4: 11-32434909-CAGCT-C
• MyVariant Identifiers: chr11:g.32456456_32456459del (hg19) ; chr11:g.32434910_32434913del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434910_32434913del , CM000673.2:g.32434910_32434913del	GRCh38
NC_000011.9:g.32456456_32456459del , CM000673.1:g.32456456_32456459del	GRCh37
NC_000011.8:g.32413032_32413035del	NCBI36
NG_009272.1:g.5629_5632del , LRG_525:g.5629_5632del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.448_451del	ENSP00000331327.5:p.Ser150GlyfsTer12
ENST00000379077.9:c.448_451del	ENSP00000368368.5:p.Ser150GlyfsTer12
ENST00000448076.9:c.448_451del	ENSP00000413452.5:p.Ser150GlyfsTer12
ENST00000452863.10:c.448_451del MANE Select	ENSP00000415516.5:p.Ser150GlyfsTer12
ENST00000639563.3:c.448_451del	ENSP00000492269.3:p.Ser150GlyfsTer12
ENST00000332351.7:c.433_436del	ENSP00000331327.3:p.Ser145GlyfsTer12
ENST00000379077.7:c.433_436del	ENSP00000368368.3:p.Ser145GlyfsTer12
ENST00000448076.7:c.433_436del	ENSP00000413452.3:p.Ser145GlyfsTer12
ENST00000452863.7:c.433_436del	ENSP00000415516.3:p.Ser145GlyfsTer12
NM_000378.4:c.433_436del	NP_000369.3:p.Ser145GlyfsTer12
NM_024424.3:c.433_436del	NP_077742.2:p.Ser145GlyfsTer12
NM_024426.4:c.433_436del	NP_077744.3:p.Ser145GlyfsTer12
NM_000378.5:c.448_451del	NP_000369.4:p.Ser150GlyfsTer12
NM_024424.4:c.448_451del	NP_077742.3:p.Ser150GlyfsTer12
NM_024426.5:c.448_451del	NP_077744.4:p.Ser150GlyfsTer12
NR_160306.1:n.627_630del
NM_000378.6:c.448_451del	NP_000369.4:p.Ser150GlyfsTer12
NM_024424.5:c.448_451del	NP_077742.3:p.Ser150GlyfsTer12
NM_024426.6:c.448_451del MANE Select	NP_077744.4:p.Ser150GlyfsTer12