Canonical Allele Identifier: CA064802

Gene: WT1

Linked Data

• ClinVar Variation Id: 576824
• ClinVar RCV Id: RCV000699416 ; RCV003465609
• dbSNP Id: rs770519620
• ExAC: 11:32456618 AGCC / A
• gnomAD v2: 11-32456618-AGCC-A
• gnomAD v3: 11-32435072-AGCC-A
• gnomAD v4: 11-32435072-AGCC-A
• MyVariant Identifiers: chr11:g.32456619_32456621del (hg19) ; chr11:g.32435074_32435076del (hg38) ; chr11:g.32435073_32435075del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435082_32435084del , CM000673.2:g.32435082_32435084del	GRCh38
NC_000011.9:g.32456628_32456630del , CM000673.1:g.32456628_32456630del	GRCh37
NC_000011.8:g.32413204_32413206del	NCBI36
NG_009272.1:g.5467_5469del , LRG_525:g.5467_5469del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.286_288del	ENSP00000331327.5:p.Gly96del
ENST00000379077.9:c.286_288del	ENSP00000368368.5:p.Gly96del
ENST00000448076.9:c.286_288del	ENSP00000413452.5:p.Gly96del
ENST00000452863.10:c.286_288del MANE Select	ENSP00000415516.5:p.Gly96del
ENST00000639563.3:c.286_288del	ENSP00000492269.3:p.Gly96del
ENST00000332351.7:c.271_273del	ENSP00000331327.3:p.Gly91del
ENST00000379077.7:c.271_273del	ENSP00000368368.3:p.Gly91del
ENST00000448076.7:c.271_273del	ENSP00000413452.3:p.Gly91del
ENST00000452863.7:c.271_273del	ENSP00000415516.3:p.Gly91del
NM_000378.4:c.271_273del	NP_000369.3:p.Gly91del
NM_024424.3:c.271_273del	NP_077742.2:p.Gly91del
NM_024426.4:c.271_273del	NP_077744.3:p.Gly91del
NM_000378.5:c.286_288del	NP_000369.4:p.Gly96del
NM_024424.4:c.286_288del	NP_077742.3:p.Gly96del
NM_024426.5:c.286_288del	NP_077744.4:p.Gly96del
NR_160306.1:n.465_467del
NM_000378.6:c.286_288del	NP_000369.4:p.Gly96del
NM_024424.5:c.286_288del	NP_077742.3:p.Gly96del
NM_024426.6:c.286_288del MANE Select	NP_077744.4:p.Gly96del