Canonical Allele Identifier: CA2499220923

Gene: WT1

Linked Data

• ClinVar Variation Id: 1063046
• ClinVar RCV Id: RCV001372846
• dbSNP Id: rs1853451296
• gnomAD v4: 11-32434953-GGGTGGCGGCGGAGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434964_32434978del , CM000673.2:g.32434964_32434978del	GRCh38
NC_000011.9:g.32456510_32456524del , CM000673.1:g.32456510_32456524del	GRCh37
NC_000011.8:g.32413086_32413100del	NCBI36
NG_009272.1:g.5574_5588del , LRG_525:g.5574_5588del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.393_407del	ENSP00000331327.5:p.Ala132_Pro136del
ENST00000379077.9:c.393_407del	ENSP00000368368.5:p.Ala132_Pro136del
ENST00000448076.9:c.393_407del	ENSP00000413452.5:p.Ala132_Pro136del
ENST00000452863.10:c.393_407del MANE Select	ENSP00000415516.5:p.Ala132_Pro136del
ENST00000639563.3:c.393_407del	ENSP00000492269.3:p.Ala132_Pro136del
ENST00000332351.7:c.378_392del	ENSP00000331327.3:p.Ala127_Pro131del
ENST00000379077.7:c.378_392del	ENSP00000368368.3:p.Ala127_Pro131del
ENST00000448076.7:c.378_392del	ENSP00000413452.3:p.Ala127_Pro131del
ENST00000452863.7:c.378_392del	ENSP00000415516.3:p.Ala127_Pro131del
NM_000378.4:c.378_392del	NP_000369.3:p.Ala127_Pro131del
NM_024424.3:c.378_392del	NP_077742.2:p.Ala127_Pro131del
NM_024426.4:c.378_392del	NP_077744.3:p.Ala127_Pro131del
NM_000378.5:c.393_407del	NP_000369.4:p.Ala132_Pro136del
NM_024424.4:c.393_407del	NP_077742.3:p.Ala132_Pro136del
NM_024426.5:c.393_407del	NP_077744.4:p.Ala132_Pro136del
NR_160306.1:n.572_586del
NM_000378.6:c.393_407del	NP_000369.4:p.Ala132_Pro136del
NM_024424.5:c.393_407del	NP_077742.3:p.Ala132_Pro136del
NM_024426.6:c.393_407del MANE Select	NP_077744.4:p.Ala132_Pro136del