Canonical Allele Identifier: CA645607359
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM24801
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880629_34880630insCTTCAGCTCAGCCGGTAGCATT , CM000683.2:g.34880629_34880630insCTTCAGCTCAGCCGGTAGCATT GRCh38
NC_000021.8:g.36252926_36252927insCTTCAGCTCAGCCGGTAGCATT , CM000683.1:g.36252926_36252927insCTTCAGCTCAGCCGGTAGCATT GRCh37
NC_000021.7:g.35174796_35174797insCTTCAGCTCAGCCGGTAGCATT NCBI36
NG_011402.2:g.1109092_1109093insGCTGAGCTGAAGAATGCTACCG , LRG_482:g.1109092_1109093insGCTGAGCTGAAGAATGCTACCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.445_446insGCTGAGCTGAAGAATGCTACCG MANE Select ENSP00000501943.1:p.Ala149GlyfsTer2
ENST00000300305.7:c.445_446insGCTGAGCTGAAGAATGCTACCG ENSP00000300305.3:p.Ala149GlyfsTer2
ENST00000344691.8:c.364_365insGCTGAGCTGAAGAATGCTACCG ENSP00000340690.4:p.Ala122GlyfsTer2
ENST00000358356.9:c.364_365insGCTGAGCTGAAGAATGCTACCG ENSP00000351123.5:p.Ala122GlyfsTer2
ENST00000399237.6:c.409_410insGCTGAGCTGAAGAATGCTACCG ENSP00000382182.2:p.Ala137GlyfsTer2
ENST00000399240.5:c.364_365insGCTGAGCTGAAGAATGCTACCG ENSP00000382184.1:p.Ala122GlyfsTer2
ENST00000437180.5:c.445_446insGCTGAGCTGAAGAATGCTACCG ENSP00000409227.1:p.Ala149GlyfsTer2
ENST00000455571.5:c.406_407insGCTGAGCTGAAGAATGCTACCG ENSP00000388189.1:p.Ala136GlyfsTer2
ENST00000482318.5:c.*35_*36insGCTGAGCTGAAGAATGCTACCG ENSP00000477067.1:n.*35_*36insGCTGAGCTGAAGAATGCTACCG
NM_001001890.2:c.364_365insGCTGAGCTGAAGAATGCTACCG NP_001001890.1:p.Ala122GlyfsTer2
NM_001122607.1:c.364_365insGCTGAGCTGAAGAATGCTACCG NP_001116079.1:p.Ala122GlyfsTer2
NM_001754.4:c.445_446insGCTGAGCTGAAGAATGCTACCG , LRG_482t1:c.445_446insGCTGAGCTGAAGAATGCTACCG NP_001745.2:p.Ala149GlyfsTer2
XM_005261068.3:c.409_410insGCTGAGCTGAAGAATGCTACCG XP_005261125.1:p.Ala137GlyfsTer2
XM_005261069.3:c.445_446insGCTGAGCTGAAGAATGCTACCG XP_005261126.1:p.Ala149GlyfsTer2
XM_011529766.1:c.445_446insGCTGAGCTGAAGAATGCTACCG XP_011528068.1:p.Ala149GlyfsTer2
XM_011529767.1:c.406_407insGCTGAGCTGAAGAATGCTACCG XP_011528069.1:p.Ala136GlyfsTer2
XM_011529768.1:c.406_407insGCTGAGCTGAAGAATGCTACCG XP_011528070.1:p.Ala136GlyfsTer2
XM_011529770.1:c.445_446insGCTGAGCTGAAGAATGCTACCG XP_011528072.1:p.Ala149GlyfsTer2
XR_937576.1:n.624_625insGCTGAGCTGAAGAATGCTACCG
XM_005261069.4:c.445_446insGCTGAGCTGAAGAATGCTACCG XP_005261126.1:p.Ala149GlyfsTer2
XM_011529766.2:c.445_446insGCTGAGCTGAAGAATGCTACCG XP_011528068.1:p.Ala149GlyfsTer2
XM_011529767.2:c.406_407insGCTGAGCTGAAGAATGCTACCG XP_011528069.1:p.Ala136GlyfsTer2
XM_011529768.2:c.406_407insGCTGAGCTGAAGAATGCTACCG XP_011528070.1:p.Ala136GlyfsTer2
XM_011529770.2:c.445_446insGCTGAGCTGAAGAATGCTACCG XP_011528072.1:p.Ala149GlyfsTer2
XM_017028487.1:c.292_293insGCTGAGCTGAAGAATGCTACCG XP_016883976.1:p.Ala98GlyfsTer2
XR_937576.2:n.671_672insGCTGAGCTGAAGAATGCTACCG
NM_001001890.3:c.364_365insGCTGAGCTGAAGAATGCTACCG NP_001001890.1:p.Ala122GlyfsTer2
NM_001122607.2:c.364_365insGCTGAGCTGAAGAATGCTACCG NP_001116079.1:p.Ala122GlyfsTer2
NM_001754.5:c.445_446insGCTGAGCTGAAGAATGCTACCG MANE Select NP_001745.2:p.Ala149GlyfsTer2
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