Canonical Allele Identifier: CA2580611885
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880560_34880562del , CM000683.2:g.34880560_34880562del GRCh38
NC_000021.8:g.36252857_36252859del , CM000683.1:g.36252857_36252859del GRCh37
NC_000021.7:g.35174727_35174729del NCBI36
NG_011402.2:g.1109152_1109154del , LRG_482:g.1109152_1109154del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.505_507del MANE Select ENSP00000501943.1:p.Arg169del
ENST00000300305.7:c.505_507del ENSP00000300305.3:p.Arg169del
ENST00000344691.8:c.424_426del ENSP00000340690.4:p.Arg142del
ENST00000358356.9:c.424_426del ENSP00000351123.5:p.Arg142del
ENST00000399237.6:c.469_471del ENSP00000382182.2:p.Arg157del
ENST00000399240.5:c.424_426del ENSP00000382184.1:p.Arg142del
ENST00000437180.5:c.505_507del ENSP00000409227.1:p.Arg169del
ENST00000482318.5:c.*95_*97del ENSP00000477067.1:n.*95_*97del
NM_001001890.2:c.424_426del NP_001001890.1:p.Arg142del
NM_001122607.1:c.424_426del NP_001116079.1:p.Arg142del
NM_001754.4:c.505_507del , LRG_482t1:c.505_507del NP_001745.2:p.Arg169del
XM_005261068.3:c.469_471del XP_005261125.1:p.Arg157del
XM_005261069.3:c.505_507del XP_005261126.1:p.Arg169del
XM_011529766.1:c.505_507del XP_011528068.1:p.Arg169del
XM_011529767.1:c.466_468del XP_011528069.1:p.Arg156del
XM_011529768.1:c.466_468del XP_011528070.1:p.Arg156del
XM_011529770.1:c.505_507del XP_011528072.1:p.Arg169del
XR_937576.1:n.684_686del
XM_005261069.4:c.505_507del XP_005261126.1:p.Arg169del
XM_011529766.2:c.505_507del XP_011528068.1:p.Arg169del
XM_011529767.2:c.466_468del XP_011528069.1:p.Arg156del
XM_011529768.2:c.466_468del XP_011528070.1:p.Arg156del
XM_011529770.2:c.505_507del XP_011528072.1:p.Arg169del
XM_017028487.1:c.352_354del XP_016883976.1:p.Arg118del
XR_937576.2:n.731_733del
NM_001001890.3:c.424_426del NP_001001890.1:p.Arg142del
NM_001122607.2:c.424_426del NP_001116079.1:p.Arg142del
NM_001754.5:c.505_507del MANE Select NP_001745.2:p.Arg169del