Canonical Allele Identifier: CA2017999289
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886954del , CM000683.2:g.34886954del GRCh38
NC_000021.8:g.36259251del , CM000683.1:g.36259251del GRCh37
NC_000021.7:g.35181121del NCBI36
NG_011402.2:g.1102759del , LRG_482:g.1102759del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.241del MANE Select ENSP00000501943.1:p.Val81CysfsTer?
ENST00000300305.7:c.241del ENSP00000300305.3:p.Val81CysfsTer?
ENST00000344691.8:c.160del ENSP00000340690.4:p.Val54CysfsTer?
ENST00000358356.9:c.160del ENSP00000351123.5:p.Val54CysfsTer?
ENST00000399237.6:c.205del ENSP00000382182.2:p.Val69CysfsTer?
ENST00000399240.5:c.160del ENSP00000382184.1:p.Val54CysfsTer?
ENST00000437180.5:c.241del ENSP00000409227.1:p.Val81CysfsTer?
ENST00000455571.5:c.202del ENSP00000388189.1:p.Val68CysfsTer?
ENST00000482318.5:c.59-6240del ENSP00000477067.1:n.59-6240del
NM_001001890.2:c.160del NP_001001890.1:p.Val54CysfsTer?
NM_001122607.1:c.160del NP_001116079.1:p.Val54CysfsTer?
NM_001754.4:c.241del , LRG_482t1:c.241del NP_001745.2:p.Val81CysfsTer?
XM_005261068.3:c.205del XP_005261125.1:p.Val69CysfsTer?
XM_005261069.3:c.241del XP_005261126.1:p.Val81CysfsTer?
XM_011529766.1:c.241del XP_011528068.1:p.Val81CysfsTer?
XM_011529767.1:c.202del XP_011528069.1:p.Val68CysfsTer?
XM_011529768.1:c.202del XP_011528070.1:p.Val68CysfsTer?
XM_011529770.1:c.241del XP_011528072.1:p.Val81CysfsTer?
XR_937576.1:n.420del
XM_005261069.4:c.241del XP_005261126.1:p.Val81CysfsTer?
XM_011529766.2:c.241del XP_011528068.1:p.Val81CysfsTer?
XM_011529767.2:c.202del XP_011528069.1:p.Val68CysfsTer?
XM_011529768.2:c.202del XP_011528070.1:p.Val68CysfsTer?
XM_011529770.2:c.241del XP_011528072.1:p.Val81CysfsTer?
XM_017028487.1:c.88del XP_016883976.1:p.Val30CysfsTer?
XR_937576.2:n.467del
NM_001001890.3:c.160del NP_001001890.1:p.Val54CysfsTer?
NM_001122607.2:c.160del NP_001116079.1:p.Val54CysfsTer?
NM_001754.5:c.241del MANE Select NP_001745.2:p.Val81CysfsTer?