Canonical Allele Identifier: CA645607444
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886922_34886923insA , CM000683.2:g.34886922_34886923insA GRCh38
NC_000021.8:g.36259219_36259220insA , CM000683.1:g.36259219_36259220insA GRCh37
NC_000021.7:g.35181089_35181090insA NCBI36
NG_011402.2:g.1102789_1102790insT , LRG_482:g.1102789_1102790insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.271_272insT MANE Select ENSP00000501943.1:p.Arg91LeufsTer?
ENST00000300305.7:c.271_272insT ENSP00000300305.3:p.Arg91LeufsTer?
ENST00000344691.8:c.190_191insT ENSP00000340690.4:p.Arg64LeufsTer?
ENST00000358356.9:c.190_191insT ENSP00000351123.5:p.Arg64LeufsTer?
ENST00000399237.6:c.235_236insT ENSP00000382182.2:p.Arg79LeufsTer?
ENST00000399240.5:c.190_191insT ENSP00000382184.1:p.Arg64LeufsTer?
ENST00000437180.5:c.271_272insT ENSP00000409227.1:p.Arg91LeufsTer?
ENST00000455571.5:c.232_233insT ENSP00000388189.1:p.Arg78LeufsTer?
ENST00000482318.5:c.59-6210_59-6209insT ENSP00000477067.1:n.59-6210_59-6209insT
NM_001001890.2:c.190_191insT NP_001001890.1:p.Arg64LeufsTer?
NM_001122607.1:c.190_191insT NP_001116079.1:p.Arg64LeufsTer?
NM_001754.4:c.271_272insT , LRG_482t1:c.271_272insT NP_001745.2:p.Arg91LeufsTer?
XM_005261068.3:c.235_236insT XP_005261125.1:p.Arg79LeufsTer?
XM_005261069.3:c.271_272insT XP_005261126.1:p.Arg91LeufsTer?
XM_011529766.1:c.271_272insT XP_011528068.1:p.Arg91LeufsTer?
XM_011529767.1:c.232_233insT XP_011528069.1:p.Arg78LeufsTer?
XM_011529768.1:c.232_233insT XP_011528070.1:p.Arg78LeufsTer?
XM_011529770.1:c.271_272insT XP_011528072.1:p.Arg91LeufsTer?
XR_937576.1:n.450_451insT
XM_005261069.4:c.271_272insT XP_005261126.1:p.Arg91LeufsTer?
XM_011529766.2:c.271_272insT XP_011528068.1:p.Arg91LeufsTer?
XM_011529767.2:c.232_233insT XP_011528069.1:p.Arg78LeufsTer?
XM_011529768.2:c.232_233insT XP_011528070.1:p.Arg78LeufsTer?
XM_011529770.2:c.271_272insT XP_011528072.1:p.Arg91LeufsTer?
XM_017028487.1:c.118_119insT XP_016883976.1:p.Arg40LeufsTer?
XR_937576.2:n.497_498insT
NM_001001890.3:c.190_191insT NP_001001890.1:p.Arg64LeufsTer?
NM_001122607.2:c.190_191insT NP_001116079.1:p.Arg64LeufsTer?
NM_001754.5:c.271_272insT MANE Select NP_001745.2:p.Arg91LeufsTer?