Canonical Allele Identifier: CA2580615657

Gene: WT1

Linked Data

• ClinVar Variation Id: 1448032
• ClinVar RCV Id: RCV002012045 ; RCV004010975
• dbSNP Id: rs770519620
• gnomAD v4: 11-32435072-A-AGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435082_32435084dup , CM000673.2:g.32435082_32435084dup	GRCh38
NC_000011.9:g.32456628_32456630dup , CM000673.1:g.32456628_32456630dup	GRCh37
NC_000011.8:g.32413204_32413206dup	NCBI36
NG_009272.1:g.5467_5469dup , LRG_525:g.5467_5469dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.286_288dup	ENSP00000331327.5:p.Gly96_Cys97insGly
ENST00000379077.9:c.286_288dup	ENSP00000368368.5:p.Gly96_Cys97insGly
ENST00000448076.9:c.286_288dup	ENSP00000413452.5:p.Gly96_Cys97insGly
ENST00000452863.10:c.286_288dup MANE Select	ENSP00000415516.5:p.Gly96_Cys97insGly
ENST00000639563.3:c.286_288dup	ENSP00000492269.3:p.Gly96_Cys97insGly
ENST00000332351.7:c.271_273dup	ENSP00000331327.3:p.Gly91_Cys92insGly
ENST00000379077.7:c.271_273dup	ENSP00000368368.3:p.Gly91_Cys92insGly
ENST00000448076.7:c.271_273dup	ENSP00000413452.3:p.Gly91_Cys92insGly
ENST00000452863.7:c.271_273dup	ENSP00000415516.3:p.Gly91_Cys92insGly
NM_000378.4:c.271_273dup	NP_000369.3:p.Gly91_Cys92insGly
NM_024424.3:c.271_273dup	NP_077742.2:p.Gly91_Cys92insGly
NM_024426.4:c.271_273dup	NP_077744.3:p.Gly91_Cys92insGly
NM_000378.5:c.286_288dup	NP_000369.4:p.Gly96_Cys97insGly
NM_024424.4:c.286_288dup	NP_077742.3:p.Gly96_Cys97insGly
NM_024426.5:c.286_288dup	NP_077744.4:p.Gly96_Cys97insGly
NR_160306.1:n.465_467dup
NM_000378.6:c.286_288dup	NP_000369.4:p.Gly96_Cys97insGly
NM_024424.5:c.286_288dup	NP_077742.3:p.Gly96_Cys97insGly
NM_024426.6:c.286_288dup MANE Select	NP_077744.4:p.Gly96_Cys97insGly