Canonical Allele Identifier: CA5934336

Gene: WT1

Linked Data

• ClinVar Variation Id: 406690
• ClinVar RCV Id: RCV000461389 ; RCV000761054 ; RCV002256255 ; RCV003231488
• dbSNP Id: rs760304811
• ExAC: 11:32456484 A / AGGC
• gnomAD v2: 11-32456484-A-AGGC
• gnomAD v3: 11-32434938-A-AGGC
• gnomAD v4: 11-32434938-A-AGGC
• MyVariant Identifiers: chr11:g.32456485_32456487dupGGC (hg19) ; chr11:g.32456487_32456488insGGC (hg19) ; chr11:g.32456484_32456485insGGC (hg19) ; chr11:g.32434939_32434941dupGGC (hg38) ; chr11:g.32434938_32434939insGGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32434950_32434952dup , CM000673.2:g.32434950_32434952dup	GRCh38
NC_000011.9:g.32456496_32456498dup , CM000673.1:g.32456496_32456498dup	GRCh37
NC_000011.8:g.32413072_32413074dup	NCBI36
NG_009272.1:g.5601_5603dup , LRG_525:g.5601_5603dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.420_422dup	ENSP00000331327.5:p.Pro141_His142insPro
ENST00000379077.9:c.420_422dup	ENSP00000368368.5:p.Pro141_His142insPro
ENST00000448076.9:c.420_422dup	ENSP00000413452.5:p.Pro141_His142insPro
ENST00000452863.10:c.420_422dup MANE Select	ENSP00000415516.5:p.Pro141_His142insPro
ENST00000639563.3:c.420_422dup	ENSP00000492269.3:p.Pro141_His142insPro
ENST00000332351.7:c.405_407dup	ENSP00000331327.3:p.Pro136_His137insPro
ENST00000379077.7:c.405_407dup	ENSP00000368368.3:p.Pro136_His137insPro
ENST00000448076.7:c.405_407dup	ENSP00000413452.3:p.Pro136_His137insPro
ENST00000452863.7:c.405_407dup	ENSP00000415516.3:p.Pro136_His137insPro
NM_000378.4:c.405_407dup	NP_000369.3:p.Pro136_His137insPro
NM_024424.3:c.405_407dup	NP_077742.2:p.Pro136_His137insPro
NM_024426.4:c.405_407dup	NP_077744.3:p.Pro136_His137insPro
NM_000378.5:c.420_422dup	NP_000369.4:p.Pro141_His142insPro
NM_024424.4:c.420_422dup	NP_077742.3:p.Pro141_His142insPro
NM_024426.5:c.420_422dup	NP_077744.4:p.Pro141_His142insPro
NR_160306.1:n.599_601dup
NM_000378.6:c.420_422dup	NP_000369.4:p.Pro141_His142insPro
NM_024424.5:c.420_422dup	NP_077742.3:p.Pro141_His142insPro
NM_024426.6:c.420_422dup MANE Select	NP_077744.4:p.Pro141_His142insPro