Canonical Allele Identifier: CA645607463
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM24754

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887027_34887081del , CM000683.2:g.34887027_34887081del GRCh38
NC_000021.8:g.36259324_36259378del , CM000683.1:g.36259324_36259378del GRCh37
NC_000021.7:g.35181194_35181248del NCBI36
NG_011402.2:g.1102637_1102691del , LRG_482:g.1102637_1102691del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.119_173del MANE Select ENSP00000501943.1:p.Phe40TrpfsTer14
ENST00000300305.7:c.119_173del ENSP00000300305.3:p.Phe40TrpfsTer14
ENST00000344691.8:c.38_92del ENSP00000340690.4:p.Phe13TrpfsTer14
ENST00000358356.9:c.38_92del ENSP00000351123.5:p.Phe13TrpfsTer14
ENST00000399237.6:c.83_137del ENSP00000382182.2:p.Phe28TrpfsTer14
ENST00000399240.5:c.38_92del ENSP00000382184.1:p.Phe13TrpfsTer14
ENST00000437180.5:c.119_173del ENSP00000409227.1:p.Phe40TrpfsTer14
ENST00000455571.5:c.80_134del ENSP00000388189.1:p.Phe27TrpfsTer14
ENST00000482318.5:c.59-6362_59-6308del ENSP00000477067.1:n.59-6362_59-6308del
NM_001001890.2:c.38_92del NP_001001890.1:p.Phe13TrpfsTer14
NM_001122607.1:c.38_92del NP_001116079.1:p.Phe13TrpfsTer14
NM_001754.4:c.119_173del , LRG_482t1:c.119_173del NP_001745.2:p.Phe40TrpfsTer14
XM_005261068.3:c.83_137del XP_005261125.1:p.Phe28TrpfsTer14
XM_005261069.3:c.119_173del XP_005261126.1:p.Phe40TrpfsTer14
XM_011529766.1:c.119_173del XP_011528068.1:p.Phe40TrpfsTer14
XM_011529767.1:c.80_134del XP_011528069.1:p.Phe27TrpfsTer14
XM_011529768.1:c.80_134del XP_011528070.1:p.Phe27TrpfsTer14
XM_011529770.1:c.119_173del XP_011528072.1:p.Phe40TrpfsTer14
XR_937576.1:n.298_352del
XM_005261069.4:c.119_173del XP_005261126.1:p.Phe40TrpfsTer14
XM_011529766.2:c.119_173del XP_011528068.1:p.Phe40TrpfsTer14
XM_011529767.2:c.80_134del XP_011528069.1:p.Phe27TrpfsTer14
XM_011529768.2:c.80_134del XP_011528070.1:p.Phe27TrpfsTer14
XM_011529770.2:c.119_173del XP_011528072.1:p.Phe40TrpfsTer14
XM_017028487.1:c.-35_20del
XR_937576.2:n.345_399del
NM_001001890.3:c.38_92del NP_001001890.1:p.Phe13TrpfsTer14
NM_001122607.2:c.38_92del NP_001116079.1:p.Phe13TrpfsTer14
NM_001754.5:c.119_173del MANE Select NP_001745.2:p.Phe40TrpfsTer14