Canonical Allele Identifier: CA645584490
Gene: WT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32435022_32435023insGGCAA , CM000673.2:g.32435022_32435023insGGCAA GRCh38
NC_000011.9:g.32456568_32456569insGGCAA , CM000673.1:g.32456568_32456569insGGCAA GRCh37
NC_000011.8:g.32413144_32413145insGGCAA NCBI36
NG_009272.1:g.5520_5521insTGCCT , LRG_525:g.5520_5521insTGCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000332351.9:c.339_340insTGCCT ENSP00000331327.5:p.Ala114CysfsTer?
ENST00000379077.9:c.339_340insTGCCT ENSP00000368368.5:p.Ala114CysfsTer?
ENST00000448076.9:c.339_340insTGCCT ENSP00000413452.5:p.Ala114CysfsTer?
ENST00000452863.10:c.339_340insTGCCT MANE Select ENSP00000415516.5:p.Ala114CysfsTer?
ENST00000639563.3:c.339_340insTGCCT ENSP00000492269.3:p.Ala114CysfsTer?
ENST00000332351.7:c.324_325insTGCCT ENSP00000331327.3:p.Ala109CysfsTer?
ENST00000379077.7:c.324_325insTGCCT ENSP00000368368.3:p.Ala109CysfsTer?
ENST00000448076.7:c.324_325insTGCCT ENSP00000413452.3:p.Ala109CysfsTer?
ENST00000452863.7:c.324_325insTGCCT ENSP00000415516.3:p.Ala109CysfsTer?
NM_000378.4:c.324_325insTGCCT NP_000369.3:p.Ala109CysfsTer?
NM_024424.3:c.324_325insTGCCT NP_077742.2:p.Ala109CysfsTer?
NM_024426.4:c.324_325insTGCCT NP_077744.3:p.Ala109CysfsTer?
NM_000378.5:c.339_340insTGCCT NP_000369.4:p.Ala114CysfsTer?
NM_024424.4:c.339_340insTGCCT NP_077742.3:p.Ala114CysfsTer?
NM_024426.5:c.339_340insTGCCT NP_077744.4:p.Ala114CysfsTer?
NR_160306.1:n.518_519insTGCCT
NM_000378.6:c.339_340insTGCCT NP_000369.4:p.Ala114CysfsTer?
NM_024424.5:c.339_340insTGCCT NP_077742.3:p.Ala114CysfsTer?
NM_024426.6:c.339_340insTGCCT MANE Select NP_077744.4:p.Ala114CysfsTer?