Canonical Allele Identifier: CA2387297159
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886940_34886967delinsTGGTCGGCCAGCACCTCCACCATGCTGC , CM000683.2:g.34886940_34886967delinsTGGTCGGCCAGCACCTCCACCATGCTGC GRCh38
NC_000021.8:g.36259237_36259264delinsTGGTCGGCCAGCACCTCCACCATGCTGC , CM000683.1:g.36259237_36259264delinsTGGTCGGCCAGCACCTCCACCATGCTGC GRCh37
NC_000021.7:g.35181107_35181134delinsTGGTCGGCCAGCACCTCCACCATGCTGC NCBI36
NG_011402.2:g.1102745_1102772delinsGCAGCATGGTGGAGGTGCTGGCCGACCA , LRG_482:g.1102745_1102772delinsGCAGCATGGTGGAGGTGCTGGCCGACCA

Transcript Alleles

HGVS Amino-acid change
ENST00000675419.1:c.227_254delinsGCAGCATGGTGGAGGTGCTGGCCGACCA MANE Select ENSP00000501943.1:p.Arg76=
ENST00000300305.7:c.227_254delinsGCAGCATGGTGGAGGTGCTGGCCGACCA ENSP00000300305.3:p.Arg76=
ENST00000344691.8:c.146_173delinsGCAGCATGGTGGAGGTGCTGGCCGACCA ENSP00000340690.4:p.Arg49=
ENST00000358356.9:c.146_173delinsGCAGCATGGTGGAGGTGCTGGCCGACCA ENSP00000351123.5:p.Arg49=
ENST00000399237.6:c.191_218delinsGCAGCATGGTGGAGGTGCTGGCCGACCA ENSP00000382182.2:p.Arg64=
ENST00000399240.5:c.146_173delinsGCAGCATGGTGGAGGTGCTGGCCGACCA ENSP00000382184.1:p.Arg49=
ENST00000437180.5:c.227_254delinsGCAGCATGGTGGAGGTGCTGGCCGACCA ENSP00000409227.1:p.Arg76=
ENST00000455571.5:c.188_215delinsGCAGCATGGTGGAGGTGCTGGCCGACCA ENSP00000388189.1:p.Arg63=
ENST00000482318.5:c.59-6254_59-6227delinsGCAGCATGGTGGAGGTGCTGGCCGACCA ENSP00000477067.1:n.59-6254_59-6227delinsGCAGCATGGTGGAGGTGCTG...
NM_001001890.2:c.146_173delinsGCAGCATGGTGGAGGTGCTGGCCGACCA NP_001001890.1:p.Arg49=
NM_001122607.1:c.146_173delinsGCAGCATGGTGGAGGTGCTGGCCGACCA NP_001116079.1:p.Arg49=
NM_001754.4:c.227_254delinsGCAGCATGGTGGAGGTGCTGGCCGACCA , LRG_482t1:c.227_254delinsGCAGCATGGTGGAGGTGCTGGCCGACCA NP_001745.2:p.Arg76=
XM_005261068.3:c.191_218delinsGCAGCATGGTGGAGGTGCTGGCCGACCA XP_005261125.1:p.Arg64=
XM_005261069.3:c.227_254delinsGCAGCATGGTGGAGGTGCTGGCCGACCA XP_005261126.1:p.Arg76=
XM_011529766.1:c.227_254delinsGCAGCATGGTGGAGGTGCTGGCCGACCA XP_011528068.1:p.Arg76=
XM_011529767.1:c.188_215delinsGCAGCATGGTGGAGGTGCTGGCCGACCA XP_011528069.1:p.Arg63=
XM_011529768.1:c.188_215delinsGCAGCATGGTGGAGGTGCTGGCCGACCA XP_011528070.1:p.Arg63=
XM_011529770.1:c.227_254delinsGCAGCATGGTGGAGGTGCTGGCCGACCA XP_011528072.1:p.Arg76=
XR_937576.1:n.406_433delinsGCAGCATGGTGGAGGTGCTGGCCGACCA
XM_005261069.4:c.227_254delinsGCAGCATGGTGGAGGTGCTGGCCGACCA XP_005261126.1:p.Arg76=
XM_011529766.2:c.227_254delinsGCAGCATGGTGGAGGTGCTGGCCGACCA XP_011528068.1:p.Arg76=
XM_011529767.2:c.188_215delinsGCAGCATGGTGGAGGTGCTGGCCGACCA XP_011528069.1:p.Arg63=
XM_011529768.2:c.188_215delinsGCAGCATGGTGGAGGTGCTGGCCGACCA XP_011528070.1:p.Arg63=
XM_011529770.2:c.227_254delinsGCAGCATGGTGGAGGTGCTGGCCGACCA XP_011528072.1:p.Arg76=
XM_017028487.1:c.74_101delinsGCAGCATGGTGGAGGTGCTGGCCGACCA XP_016883976.1:p.Arg25=
XR_937576.2:n.453_480delinsGCAGCATGGTGGAGGTGCTGGCCGACCA
NM_001001890.3:c.146_173delinsGCAGCATGGTGGAGGTGCTGGCCGACCA NP_001001890.1:p.Arg49=
NM_001122607.2:c.146_173delinsGCAGCATGGTGGAGGTGCTGGCCGACCA NP_001116079.1:p.Arg49=
NM_001754.5:c.227_254delinsGCAGCATGGTGGAGGTGCTGGCCGACCA MANE Select NP_001745.2:p.Arg76=