Canonical Allele Identifier: CA016460
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3484
ClinVar RCV Id: RCV000003653
dbSNP Id: rs587776573

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32417638_32417654del , CM000673.2:g.32417638_32417654del GRCh38
NC_000011.9:g.32439184_32439200del , CM000673.1:g.32439184_32439200del GRCh37
NC_000011.8:g.32395760_32395776del NCBI36
NG_009272.1:g.22893_22909del , LRG_525:g.22893_22909del

Transcript Alleles

HGVS Amino-acid change
ENST00000332351.9:c.893_909del ENSP00000331327.5:p.Asn298IlefsTer4
ENST00000379077.9:c.893_909del ENSP00000368368.5:p.Asn298IlefsTer4
ENST00000379079.8:c.242_258del ENSP00000368370.2:p.Asn81IlefsTer4
ENST00000448076.9:c.893_909del ENSP00000413452.5:p.Asn298IlefsTer4
ENST00000452863.10:c.893_909del MANE Select ENSP00000415516.5:p.Asn298IlefsTer4
ENST00000639563.3:c.893_909del ENSP00000492269.3:p.Asn298IlefsTer4
ENST00000640146.2:c.269_285del ENSP00000491984.2:p.Asn90IlefsTer4
ENST00000332351.7:c.878_894del ENSP00000331327.3:p.Asn293IlefsTer4
ENST00000379077.7:c.878_894del ENSP00000368368.3:p.Asn293IlefsTer4
ENST00000379079.6:c.242_258del ENSP00000368370.2:p.Asn81IlefsTer4
ENST00000448076.7:c.878_894del ENSP00000413452.3:p.Asn293IlefsTer4
ENST00000452863.7:c.878_894del ENSP00000415516.3:p.Asn293IlefsTer4
ENST00000527775.1:c.131_147del ENSP00000435351.1:p.Asn44IlefsTer4
ENST00000530998.5:c.242_258del ENSP00000435307.1:p.Asn81IlefsTer4
NM_000378.4:c.878_894del NP_000369.3:p.Asn293IlefsTer4
NM_001198551.1:c.242_258del , LRG_525t2:c.242_258del NP_001185480.1:p.Asn81IlefsTer4
NM_001198552.1:c.242_258del NP_001185481.1:p.Asn81IlefsTer4
NM_024424.3:c.878_894del NP_077742.2:p.Asn293IlefsTer4
NM_024426.4:c.878_894del NP_077744.3:p.Asn293IlefsTer4
NM_000378.5:c.893_909del NP_000369.4:p.Asn298IlefsTer4
NM_024424.4:c.893_909del NP_077742.3:p.Asn298IlefsTer4
NM_024426.5:c.893_909del NP_077744.4:p.Asn298IlefsTer4
NR_160306.1:n.1072_1088del
NM_000378.6:c.893_909del NP_000369.4:p.Asn298IlefsTer4
NM_001198552.2:c.242_258del NP_001185481.1:p.Asn81IlefsTer4
NM_024424.5:c.893_909del NP_077742.3:p.Asn298IlefsTer4
NM_024426.6:c.893_909del MANE Select NP_077744.4:p.Asn298IlefsTer4