Canonical Allele Identifier: CA645607357
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM6191291
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880618_34880619insCGGTAGCATTTCTCAGCTCAGC , CM000683.2:g.34880618_34880619insCGGTAGCATTTCTCAGCTCAGC GRCh38
NC_000021.8:g.36252915_36252916insCGGTAGCATTTCTCAGCTCAGC , CM000683.1:g.36252915_36252916insCGGTAGCATTTCTCAGCTCAGC GRCh37
NC_000021.7:g.35174785_35174786insCGGTAGCATTTCTCAGCTCAGC NCBI36
NG_011402.2:g.1109093_1109094insGCTGAGCTGAGAAATGCTACCG , LRG_482:g.1109093_1109094insGCTGAGCTGAGAAATGCTACCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.446_447insGCTGAGCTGAGAAATGCTACCG MANE Select ENSP00000501943.1:p.Ala150LeufsTer3
ENST00000300305.7:c.446_447insGCTGAGCTGAGAAATGCTACCG ENSP00000300305.3:p.Ala150LeufsTer3
ENST00000344691.8:c.365_366insGCTGAGCTGAGAAATGCTACCG ENSP00000340690.4:p.Ala123LeufsTer3
ENST00000358356.9:c.365_366insGCTGAGCTGAGAAATGCTACCG ENSP00000351123.5:p.Ala123LeufsTer3
ENST00000399237.6:c.410_411insGCTGAGCTGAGAAATGCTACCG ENSP00000382182.2:p.Ala138LeufsTer3
ENST00000399240.5:c.365_366insGCTGAGCTGAGAAATGCTACCG ENSP00000382184.1:p.Ala123LeufsTer3
ENST00000437180.5:c.446_447insGCTGAGCTGAGAAATGCTACCG ENSP00000409227.1:p.Ala150LeufsTer3
ENST00000455571.5:c.407_408insGCTGAGCTGAGAAATGCTACCG ENSP00000388189.1:p.Ala137LeufsTer3
ENST00000482318.5:c.*36_*37insGCTGAGCTGAGAAATGCTACCG ENSP00000477067.1:n.*36_*37insGCTGAGCTGAGAAATGCTACCG
NM_001001890.2:c.365_366insGCTGAGCTGAGAAATGCTACCG NP_001001890.1:p.Ala123LeufsTer3
NM_001122607.1:c.365_366insGCTGAGCTGAGAAATGCTACCG NP_001116079.1:p.Ala123LeufsTer3
NM_001754.4:c.446_447insGCTGAGCTGAGAAATGCTACCG , LRG_482t1:c.446_447insGCTGAGCTGAGAAATGCTACCG NP_001745.2:p.Ala150LeufsTer3
XM_005261068.3:c.410_411insGCTGAGCTGAGAAATGCTACCG XP_005261125.1:p.Ala138LeufsTer3
XM_005261069.3:c.446_447insGCTGAGCTGAGAAATGCTACCG XP_005261126.1:p.Ala150LeufsTer3
XM_011529766.1:c.446_447insGCTGAGCTGAGAAATGCTACCG XP_011528068.1:p.Ala150LeufsTer3
XM_011529767.1:c.407_408insGCTGAGCTGAGAAATGCTACCG XP_011528069.1:p.Ala137LeufsTer3
XM_011529768.1:c.407_408insGCTGAGCTGAGAAATGCTACCG XP_011528070.1:p.Ala137LeufsTer3
XM_011529770.1:c.446_447insGCTGAGCTGAGAAATGCTACCG XP_011528072.1:p.Ala150LeufsTer3
XR_937576.1:n.625_626insGCTGAGCTGAGAAATGCTACCG
XM_005261069.4:c.446_447insGCTGAGCTGAGAAATGCTACCG XP_005261126.1:p.Ala150LeufsTer3
XM_011529766.2:c.446_447insGCTGAGCTGAGAAATGCTACCG XP_011528068.1:p.Ala150LeufsTer3
XM_011529767.2:c.407_408insGCTGAGCTGAGAAATGCTACCG XP_011528069.1:p.Ala137LeufsTer3
XM_011529768.2:c.407_408insGCTGAGCTGAGAAATGCTACCG XP_011528070.1:p.Ala137LeufsTer3
XM_011529770.2:c.446_447insGCTGAGCTGAGAAATGCTACCG XP_011528072.1:p.Ala150LeufsTer3
XM_017028487.1:c.293_294insGCTGAGCTGAGAAATGCTACCG XP_016883976.1:p.Ala99LeufsTer3
XR_937576.2:n.672_673insGCTGAGCTGAGAAATGCTACCG
NM_001001890.3:c.365_366insGCTGAGCTGAGAAATGCTACCG NP_001001890.1:p.Ala123LeufsTer3
NM_001122607.2:c.365_366insGCTGAGCTGAGAAATGCTACCG NP_001116079.1:p.Ala123LeufsTer3
NM_001754.5:c.446_447insGCTGAGCTGAGAAATGCTACCG MANE Select NP_001745.2:p.Ala150LeufsTer3
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