Canonical Allele Identifier: CA2695202659
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880637del , CM000683.2:g.34880637del GRCh38
NC_000021.8:g.36252934del , CM000683.1:g.36252934del GRCh37
NC_000021.7:g.35174804del NCBI36
NG_011402.2:g.1109075del , LRG_482:g.1109075del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.428del MANE Select ENSP00000501943.1:p.Glu143GlyfsTer2
ENST00000300305.7:c.428del ENSP00000300305.3:p.Glu143GlyfsTer2
ENST00000344691.8:c.347del ENSP00000340690.4:p.Glu116GlyfsTer2
ENST00000358356.9:c.347del ENSP00000351123.5:p.Glu116GlyfsTer2
ENST00000399237.6:c.392del ENSP00000382182.2:p.Glu131GlyfsTer2
ENST00000399240.5:c.347del ENSP00000382184.1:p.Glu116GlyfsTer2
ENST00000437180.5:c.428del ENSP00000409227.1:p.Glu143GlyfsTer2
ENST00000455571.5:c.389del ENSP00000388189.1:p.Glu130GlyfsTer2
ENST00000482318.5:c.*18del ENSP00000477067.1:n.*18del
NM_001001890.2:c.347del NP_001001890.1:p.Glu116GlyfsTer2
NM_001122607.1:c.347del NP_001116079.1:p.Glu116GlyfsTer2
NM_001754.4:c.428del , LRG_482t1:c.428del NP_001745.2:p.Glu143GlyfsTer2
XM_005261068.3:c.392del XP_005261125.1:p.Glu131GlyfsTer2
XM_005261069.3:c.428del XP_005261126.1:p.Glu143GlyfsTer2
XM_011529766.1:c.428del XP_011528068.1:p.Glu143GlyfsTer2
XM_011529767.1:c.389del XP_011528069.1:p.Glu130GlyfsTer2
XM_011529768.1:c.389del XP_011528070.1:p.Glu130GlyfsTer2
XM_011529770.1:c.428del XP_011528072.1:p.Glu143GlyfsTer2
XR_937576.1:n.607del
XM_005261069.4:c.428del XP_005261126.1:p.Glu143GlyfsTer2
XM_011529766.2:c.428del XP_011528068.1:p.Glu143GlyfsTer2
XM_011529767.2:c.389del XP_011528069.1:p.Glu130GlyfsTer2
XM_011529768.2:c.389del XP_011528070.1:p.Glu130GlyfsTer2
XM_011529770.2:c.428del XP_011528072.1:p.Glu143GlyfsTer2
XM_017028487.1:c.275del XP_016883976.1:p.Glu92GlyfsTer2
XR_937576.2:n.654del
NM_001001890.3:c.347del NP_001001890.1:p.Glu116GlyfsTer2
NM_001122607.2:c.347del NP_001116079.1:p.Glu116GlyfsTer2
NM_001754.5:c.428del MANE Select NP_001745.2:p.Glu143GlyfsTer2