Canonical Allele Identifier: CA645607370
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM24780
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880644_34880645insAAGGAGTCAGCCGA , CM000683.2:g.34880644_34880645insAAGGAGTCAGCCGA GRCh38
NC_000021.8:g.36252941_36252942insAAGGAGTCAGCCGA , CM000683.1:g.36252941_36252942insAAGGAGTCAGCCGA GRCh37
NC_000021.7:g.35174811_35174812insAAGGAGTCAGCCGA NCBI36
NG_011402.2:g.1109075_1109076insCTCCTTTCGGCTGA , LRG_482:g.1109075_1109076insCTCCTTTCGGCTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.428_429insCTCCTTTCGGCTGA MANE Select ENSP00000501943.1:p.Glu143AspfsTer7
ENST00000300305.7:c.428_429insCTCCTTTCGGCTGA ENSP00000300305.3:p.Glu143AspfsTer7
ENST00000344691.8:c.347_348insCTCCTTTCGGCTGA ENSP00000340690.4:p.Glu116AspfsTer7
ENST00000358356.9:c.347_348insCTCCTTTCGGCTGA ENSP00000351123.5:p.Glu116AspfsTer7
ENST00000399237.6:c.392_393insCTCCTTTCGGCTGA ENSP00000382182.2:p.Glu131AspfsTer7
ENST00000399240.5:c.347_348insCTCCTTTCGGCTGA ENSP00000382184.1:p.Glu116AspfsTer7
ENST00000437180.5:c.428_429insCTCCTTTCGGCTGA ENSP00000409227.1:p.Glu143AspfsTer7
ENST00000455571.5:c.389_390insCTCCTTTCGGCTGA ENSP00000388189.1:p.Glu130AspfsTer7
ENST00000482318.5:c.*18_*19insCTCCTTTCGGCTGA ENSP00000477067.1:n.*18_*19insCTCCTTTCGGCTGA
NM_001001890.2:c.347_348insCTCCTTTCGGCTGA NP_001001890.1:p.Glu116AspfsTer7
NM_001122607.1:c.347_348insCTCCTTTCGGCTGA NP_001116079.1:p.Glu116AspfsTer7
NM_001754.4:c.428_429insCTCCTTTCGGCTGA , LRG_482t1:c.428_429insCTCCTTTCGGCTGA NP_001745.2:p.Glu143AspfsTer7
XM_005261068.3:c.392_393insCTCCTTTCGGCTGA XP_005261125.1:p.Glu131AspfsTer7
XM_005261069.3:c.428_429insCTCCTTTCGGCTGA XP_005261126.1:p.Glu143AspfsTer7
XM_011529766.1:c.428_429insCTCCTTTCGGCTGA XP_011528068.1:p.Glu143AspfsTer7
XM_011529767.1:c.389_390insCTCCTTTCGGCTGA XP_011528069.1:p.Glu130AspfsTer7
XM_011529768.1:c.389_390insCTCCTTTCGGCTGA XP_011528070.1:p.Glu130AspfsTer7
XM_011529770.1:c.428_429insCTCCTTTCGGCTGA XP_011528072.1:p.Glu143AspfsTer7
XR_937576.1:n.607_608insCTCCTTTCGGCTGA
XM_005261069.4:c.428_429insCTCCTTTCGGCTGA XP_005261126.1:p.Glu143AspfsTer7
XM_011529766.2:c.428_429insCTCCTTTCGGCTGA XP_011528068.1:p.Glu143AspfsTer7
XM_011529767.2:c.389_390insCTCCTTTCGGCTGA XP_011528069.1:p.Glu130AspfsTer7
XM_011529768.2:c.389_390insCTCCTTTCGGCTGA XP_011528070.1:p.Glu130AspfsTer7
XM_011529770.2:c.428_429insCTCCTTTCGGCTGA XP_011528072.1:p.Glu143AspfsTer7
XM_017028487.1:c.275_276insCTCCTTTCGGCTGA XP_016883976.1:p.Glu92AspfsTer7
XR_937576.2:n.654_655insCTCCTTTCGGCTGA
NM_001001890.3:c.347_348insCTCCTTTCGGCTGA NP_001001890.1:p.Glu116AspfsTer7
NM_001122607.2:c.347_348insCTCCTTTCGGCTGA NP_001116079.1:p.Glu116AspfsTer7
NM_001754.5:c.428_429insCTCCTTTCGGCTGA MANE Select NP_001745.2:p.Glu143AspfsTer7
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