Canonical Allele Identifier: CA645607446
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM5944802
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886925_34886926insAGGTGCG , CM000683.2:g.34886925_34886926insAGGTGCG GRCh38
NC_000021.8:g.36259222_36259223insAGGTGCG , CM000683.1:g.36259222_36259223insAGGTGCG GRCh37
NC_000021.7:g.35181092_35181093insAGGTGCG NCBI36
NG_011402.2:g.1102786_1102787insCGCACCT , LRG_482:g.1102786_1102787insCGCACCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.268_269insCGCACCT MANE Select ENSP00000501943.1:p.Val90AlafsTer?
ENST00000300305.7:c.268_269insCGCACCT ENSP00000300305.3:p.Val90AlafsTer?
ENST00000344691.8:c.187_188insCGCACCT ENSP00000340690.4:p.Val63AlafsTer?
ENST00000358356.9:c.187_188insCGCACCT ENSP00000351123.5:p.Val63AlafsTer?
ENST00000399237.6:c.232_233insCGCACCT ENSP00000382182.2:p.Val78AlafsTer?
ENST00000399240.5:c.187_188insCGCACCT ENSP00000382184.1:p.Val63AlafsTer?
ENST00000437180.5:c.268_269insCGCACCT ENSP00000409227.1:p.Val90AlafsTer?
ENST00000455571.5:c.229_230insCGCACCT ENSP00000388189.1:p.Val77AlafsTer?
ENST00000482318.5:c.59-6213_59-6212insCGCACCT ENSP00000477067.1:n.59-6213_59-6212insCGCACCT
NM_001001890.2:c.187_188insCGCACCT NP_001001890.1:p.Val63AlafsTer?
NM_001122607.1:c.187_188insCGCACCT NP_001116079.1:p.Val63AlafsTer?
NM_001754.4:c.268_269insCGCACCT , LRG_482t1:c.268_269insCGCACCT NP_001745.2:p.Val90AlafsTer?
XM_005261068.3:c.232_233insCGCACCT XP_005261125.1:p.Val78AlafsTer?
XM_005261069.3:c.268_269insCGCACCT XP_005261126.1:p.Val90AlafsTer?
XM_011529766.1:c.268_269insCGCACCT XP_011528068.1:p.Val90AlafsTer?
XM_011529767.1:c.229_230insCGCACCT XP_011528069.1:p.Val77AlafsTer?
XM_011529768.1:c.229_230insCGCACCT XP_011528070.1:p.Val77AlafsTer?
XM_011529770.1:c.268_269insCGCACCT XP_011528072.1:p.Val90AlafsTer?
XR_937576.1:n.447_448insCGCACCT
XM_005261069.4:c.268_269insCGCACCT XP_005261126.1:p.Val90AlafsTer?
XM_011529766.2:c.268_269insCGCACCT XP_011528068.1:p.Val90AlafsTer?
XM_011529767.2:c.229_230insCGCACCT XP_011528069.1:p.Val77AlafsTer?
XM_011529768.2:c.229_230insCGCACCT XP_011528070.1:p.Val77AlafsTer?
XM_011529770.2:c.268_269insCGCACCT XP_011528072.1:p.Val90AlafsTer?
XM_017028487.1:c.115_116insCGCACCT XP_016883976.1:p.Val39AlafsTer?
XR_937576.2:n.494_495insCGCACCT
NM_001001890.3:c.187_188insCGCACCT NP_001001890.1:p.Val63AlafsTer?
NM_001122607.2:c.187_188insCGCACCT NP_001116079.1:p.Val63AlafsTer?
NM_001754.5:c.268_269insCGCACCT MANE Select NP_001745.2:p.Val90AlafsTer?
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