Canonical Allele Identifier: CA645607428
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886880_34886881insC , CM000683.2:g.34886880_34886881insC GRCh38
NC_000021.8:g.36259177_36259178insC , CM000683.1:g.36259177_36259178insC GRCh37
NC_000021.7:g.35181047_35181048insC NCBI36
NG_011402.2:g.1102831_1102832insG , LRG_482:g.1102831_1102832insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.313_314insG MANE Select ENSP00000501943.1:p.His105ArgfsTer?
ENST00000300305.7:c.313_314insG ENSP00000300305.3:p.His105ArgfsTer?
ENST00000344691.8:c.232_233insG ENSP00000340690.4:p.His78ArgfsTer?
ENST00000358356.9:c.232_233insG ENSP00000351123.5:p.His78ArgfsTer?
ENST00000399237.6:c.277_278insG ENSP00000382182.2:p.His93ArgfsTer?
ENST00000399240.5:c.232_233insG ENSP00000382184.1:p.His78ArgfsTer?
ENST00000437180.5:c.313_314insG ENSP00000409227.1:p.His105ArgfsTer?
ENST00000455571.5:c.274_275insG ENSP00000388189.1:p.His92ArgfsTer?
ENST00000482318.5:c.59-6168_59-6167insG ENSP00000477067.1:n.59-6168_59-6167insG
NM_001001890.2:c.232_233insG NP_001001890.1:p.His78ArgfsTer?
NM_001122607.1:c.232_233insG NP_001116079.1:p.His78ArgfsTer?
NM_001754.4:c.313_314insG , LRG_482t1:c.313_314insG NP_001745.2:p.His105ArgfsTer?
XM_005261068.3:c.277_278insG XP_005261125.1:p.His93ArgfsTer?
XM_005261069.3:c.313_314insG XP_005261126.1:p.His105ArgfsTer?
XM_011529766.1:c.313_314insG XP_011528068.1:p.His105ArgfsTer?
XM_011529767.1:c.274_275insG XP_011528069.1:p.His92ArgfsTer?
XM_011529768.1:c.274_275insG XP_011528070.1:p.His92ArgfsTer?
XM_011529770.1:c.313_314insG XP_011528072.1:p.His105ArgfsTer?
XR_937576.1:n.492_493insG
XM_005261069.4:c.313_314insG XP_005261126.1:p.His105ArgfsTer?
XM_011529766.2:c.313_314insG XP_011528068.1:p.His105ArgfsTer?
XM_011529767.2:c.274_275insG XP_011528069.1:p.His92ArgfsTer?
XM_011529768.2:c.274_275insG XP_011528070.1:p.His92ArgfsTer?
XM_011529770.2:c.313_314insG XP_011528072.1:p.His105ArgfsTer?
XM_017028487.1:c.160_161insG XP_016883976.1:p.His54ArgfsTer?
XR_937576.2:n.539_540insG
NM_001001890.3:c.232_233insG NP_001001890.1:p.His78ArgfsTer?
NM_001122607.2:c.232_233insG NP_001116079.1:p.His78ArgfsTer?
NM_001754.5:c.313_314insG MANE Select NP_001745.2:p.His105ArgfsTer?