Canonical Allele Identifier: CA645607319
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM36060
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880562_34880563insGGGGACGCTTC , CM000683.2:g.34880562_34880563insGGGGACGCTTC GRCh38
NC_000021.8:g.36252859_36252860insGGGGACGCTTC , CM000683.1:g.36252859_36252860insGGGGACGCTTC GRCh37
NC_000021.7:g.35174729_35174730insGGGGACGCTTC NCBI36
NG_011402.2:g.1109153_1109154insCGTCCCCGAAG , LRG_482:g.1109153_1109154insCGTCCCCGAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.506_507insCGTCCCCGAAG MANE Select ENSP00000501943.1:p.Arg169SerfsTer11
ENST00000300305.7:c.506_507insCGTCCCCGAAG ENSP00000300305.3:p.Arg169SerfsTer11
ENST00000344691.8:c.425_426insCGTCCCCGAAG ENSP00000340690.4:p.Arg142SerfsTer11
ENST00000358356.9:c.425_426insCGTCCCCGAAG ENSP00000351123.5:p.Arg142SerfsTer11
ENST00000399237.6:c.470_471insCGTCCCCGAAG ENSP00000382182.2:p.Arg157SerfsTer11
ENST00000399240.5:c.425_426insCGTCCCCGAAG ENSP00000382184.1:p.Arg142SerfsTer11
ENST00000437180.5:c.506_507insCGTCCCCGAAG ENSP00000409227.1:p.Arg169SerfsTer11
ENST00000482318.5:c.*96_*97insCGTCCCCGAAG ENSP00000477067.1:n.*96_*97insCGTCCCCGAAG
NM_001001890.2:c.425_426insCGTCCCCGAAG NP_001001890.1:p.Arg142SerfsTer11
NM_001122607.1:c.425_426insCGTCCCCGAAG NP_001116079.1:p.Arg142SerfsTer11
NM_001754.4:c.506_507insCGTCCCCGAAG , LRG_482t1:c.506_507insCGTCCCCGAAG NP_001745.2:p.Arg169SerfsTer11
XM_005261068.3:c.470_471insCGTCCCCGAAG XP_005261125.1:p.Arg157SerfsTer11
XM_005261069.3:c.506_507insCGTCCCCGAAG XP_005261126.1:p.Arg169SerfsTer11
XM_011529766.1:c.506_507insCGTCCCCGAAG XP_011528068.1:p.Arg169SerfsTer11
XM_011529767.1:c.467_468insCGTCCCCGAAG XP_011528069.1:p.Arg156SerfsTer11
XM_011529768.1:c.467_468insCGTCCCCGAAG XP_011528070.1:p.Arg156SerfsTer11
XM_011529770.1:c.506_507insCGTCCCCGAAG XP_011528072.1:p.Arg169SerfsTer11
XR_937576.1:n.685_686insCGTCCCCGAAG
XM_005261069.4:c.506_507insCGTCCCCGAAG XP_005261126.1:p.Arg169SerfsTer11
XM_011529766.2:c.506_507insCGTCCCCGAAG XP_011528068.1:p.Arg169SerfsTer11
XM_011529767.2:c.467_468insCGTCCCCGAAG XP_011528069.1:p.Arg156SerfsTer11
XM_011529768.2:c.467_468insCGTCCCCGAAG XP_011528070.1:p.Arg156SerfsTer11
XM_011529770.2:c.506_507insCGTCCCCGAAG XP_011528072.1:p.Arg169SerfsTer11
XM_017028487.1:c.353_354insCGTCCCCGAAG XP_016883976.1:p.Arg118SerfsTer11
XR_937576.2:n.732_733insCGTCCCCGAAG
NM_001001890.3:c.425_426insCGTCCCCGAAG NP_001001890.1:p.Arg142SerfsTer11
NM_001122607.2:c.425_426insCGTCCCCGAAG NP_001116079.1:p.Arg142SerfsTer11
NM_001754.5:c.506_507insCGTCCCCGAAG MANE Select NP_001745.2:p.Arg169SerfsTer11
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