Canonical Allele Identifier: CA891842377
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886883delinsCA , CM000683.2:g.34886883delinsCA GRCh38
NC_000021.8:g.36259180delinsCA , CM000683.1:g.36259180delinsCA GRCh37
NC_000021.7:g.35181050delinsCA NCBI36
NG_011402.2:g.1102829delinsTG , LRG_482:g.1102829delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.311delinsTG MANE Select ENSP00000501943.1:p.Thr104MetfsTer?
ENST00000300305.7:c.311delinsTG ENSP00000300305.3:p.Thr104MetfsTer?
ENST00000344691.8:c.230delinsTG ENSP00000340690.4:p.Thr77MetfsTer?
ENST00000358356.9:c.230delinsTG ENSP00000351123.5:p.Thr77MetfsTer?
ENST00000399237.6:c.275delinsTG ENSP00000382182.2:p.Thr92MetfsTer?
ENST00000399240.5:c.230delinsTG ENSP00000382184.1:p.Thr77MetfsTer?
ENST00000437180.5:c.311delinsTG ENSP00000409227.1:p.Thr104MetfsTer?
ENST00000455571.5:c.272delinsTG ENSP00000388189.1:p.Thr91MetfsTer?
ENST00000482318.5:c.59-6170delinsTG ENSP00000477067.1:n.59-6170delinsTG
NM_001001890.2:c.230delinsTG NP_001001890.1:p.Thr77MetfsTer?
NM_001122607.1:c.230delinsTG NP_001116079.1:p.Thr77MetfsTer?
NM_001754.4:c.311delinsTG , LRG_482t1:c.311delinsTG NP_001745.2:p.Thr104MetfsTer?
XM_005261068.3:c.275delinsTG XP_005261125.1:p.Thr92MetfsTer?
XM_005261069.3:c.311delinsTG XP_005261126.1:p.Thr104MetfsTer?
XM_011529766.1:c.311delinsTG XP_011528068.1:p.Thr104MetfsTer?
XM_011529767.1:c.272delinsTG XP_011528069.1:p.Thr91MetfsTer?
XM_011529768.1:c.272delinsTG XP_011528070.1:p.Thr91MetfsTer?
XM_011529770.1:c.311delinsTG XP_011528072.1:p.Thr104MetfsTer?
XR_937576.1:n.490delinsTG
XM_005261069.4:c.311delinsTG XP_005261126.1:p.Thr104MetfsTer?
XM_011529766.2:c.311delinsTG XP_011528068.1:p.Thr104MetfsTer?
XM_011529767.2:c.272delinsTG XP_011528069.1:p.Thr91MetfsTer?
XM_011529768.2:c.272delinsTG XP_011528070.1:p.Thr91MetfsTer?
XM_011529770.2:c.311delinsTG XP_011528072.1:p.Thr104MetfsTer?
XM_017028487.1:c.158delinsTG XP_016883976.1:p.Thr53MetfsTer?
XR_937576.2:n.537delinsTG
NM_001001890.3:c.230delinsTG NP_001001890.1:p.Thr77MetfsTer?
NM_001122607.2:c.230delinsTG NP_001116079.1:p.Thr77MetfsTer?
NM_001754.5:c.311delinsTG MANE Select NP_001745.2:p.Thr104MetfsTer?