Canonical Allele Identifier: CA2654380326
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886964_34886968del , CM000683.2:g.34886964_34886968del GRCh38
NC_000021.8:g.36259261_36259265del , CM000683.1:g.36259261_36259265del GRCh37
NC_000021.7:g.35181131_35181135del NCBI36
NG_011402.2:g.1102745_1102749del , LRG_482:g.1102745_1102749del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.227_231del MANE Select ENSP00000501943.1:p.Arg76HisfsTer?
ENST00000300305.7:c.227_231del ENSP00000300305.3:p.Arg76HisfsTer?
ENST00000344691.8:c.146_150del ENSP00000340690.4:p.Arg49HisfsTer?
ENST00000358356.9:c.146_150del ENSP00000351123.5:p.Arg49HisfsTer?
ENST00000399237.6:c.191_195del ENSP00000382182.2:p.Arg64HisfsTer?
ENST00000399240.5:c.146_150del ENSP00000382184.1:p.Arg49HisfsTer?
ENST00000437180.5:c.227_231del ENSP00000409227.1:p.Arg76HisfsTer?
ENST00000455571.5:c.188_192del ENSP00000388189.1:p.Arg63HisfsTer?
ENST00000482318.5:c.59-6254_59-6250del ENSP00000477067.1:n.59-6254_59-6250del
NM_001001890.2:c.146_150del NP_001001890.1:p.Arg49HisfsTer?
NM_001122607.1:c.146_150del NP_001116079.1:p.Arg49HisfsTer?
NM_001754.4:c.227_231del , LRG_482t1:c.227_231del NP_001745.2:p.Arg76HisfsTer?
XM_005261068.3:c.191_195del XP_005261125.1:p.Arg64HisfsTer?
XM_005261069.3:c.227_231del XP_005261126.1:p.Arg76HisfsTer?
XM_011529766.1:c.227_231del XP_011528068.1:p.Arg76HisfsTer?
XM_011529767.1:c.188_192del XP_011528069.1:p.Arg63HisfsTer?
XM_011529768.1:c.188_192del XP_011528070.1:p.Arg63HisfsTer?
XM_011529770.1:c.227_231del XP_011528072.1:p.Arg76HisfsTer?
XR_937576.1:n.406_410del
XM_005261069.4:c.227_231del XP_005261126.1:p.Arg76HisfsTer?
XM_011529766.2:c.227_231del XP_011528068.1:p.Arg76HisfsTer?
XM_011529767.2:c.188_192del XP_011528069.1:p.Arg63HisfsTer?
XM_011529768.2:c.188_192del XP_011528070.1:p.Arg63HisfsTer?
XM_011529770.2:c.227_231del XP_011528072.1:p.Arg76HisfsTer?
XM_017028487.1:c.74_78del XP_016883976.1:p.Arg25HisfsTer?
XR_937576.2:n.453_457del
NM_001001890.3:c.146_150del NP_001001890.1:p.Arg49HisfsTer?
NM_001122607.2:c.146_150del NP_001116079.1:p.Arg49HisfsTer?
NM_001754.5:c.227_231del MANE Select NP_001745.2:p.Arg76HisfsTer?