Canonical Allele Identifier: CA645607465
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887027_34887028insTCAG , CM000683.2:g.34887027_34887028insTCAG GRCh38
NC_000021.8:g.36259324_36259325insTCAG , CM000683.1:g.36259324_36259325insTCAG GRCh37
NC_000021.7:g.35181194_35181195insTCAG NCBI36
NG_011402.2:g.1102684_1102685insCTGA , LRG_482:g.1102684_1102685insCTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.166_167insCTGA MANE Select ENSP00000501943.1:p.Leu56SerfsTer?
ENST00000300305.7:c.166_167insCTGA ENSP00000300305.3:p.Leu56SerfsTer?
ENST00000344691.8:c.85_86insCTGA ENSP00000340690.4:p.Leu29SerfsTer?
ENST00000358356.9:c.85_86insCTGA ENSP00000351123.5:p.Leu29SerfsTer?
ENST00000399237.6:c.130_131insCTGA ENSP00000382182.2:p.Leu44SerfsTer?
ENST00000399240.5:c.85_86insCTGA ENSP00000382184.1:p.Leu29SerfsTer?
ENST00000437180.5:c.166_167insCTGA ENSP00000409227.1:p.Leu56SerfsTer?
ENST00000455571.5:c.127_128insCTGA ENSP00000388189.1:p.Leu43SerfsTer?
ENST00000482318.5:c.59-6315_59-6314insCTGA ENSP00000477067.1:n.59-6315_59-6314insCTGA
NM_001001890.2:c.85_86insCTGA NP_001001890.1:p.Leu29SerfsTer?
NM_001122607.1:c.85_86insCTGA NP_001116079.1:p.Leu29SerfsTer?
NM_001754.4:c.166_167insCTGA , LRG_482t1:c.166_167insCTGA NP_001745.2:p.Leu56SerfsTer?
XM_005261068.3:c.130_131insCTGA XP_005261125.1:p.Leu44SerfsTer?
XM_005261069.3:c.166_167insCTGA XP_005261126.1:p.Leu56SerfsTer?
XM_011529766.1:c.166_167insCTGA XP_011528068.1:p.Leu56SerfsTer?
XM_011529767.1:c.127_128insCTGA XP_011528069.1:p.Leu43SerfsTer?
XM_011529768.1:c.127_128insCTGA XP_011528070.1:p.Leu43SerfsTer?
XM_011529770.1:c.166_167insCTGA XP_011528072.1:p.Leu56SerfsTer?
XR_937576.1:n.345_346insCTGA
XM_005261069.4:c.166_167insCTGA XP_005261126.1:p.Leu56SerfsTer?
XM_011529766.2:c.166_167insCTGA XP_011528068.1:p.Leu56SerfsTer?
XM_011529767.2:c.127_128insCTGA XP_011528069.1:p.Leu43SerfsTer?
XM_011529768.2:c.127_128insCTGA XP_011528070.1:p.Leu43SerfsTer?
XM_011529770.2:c.166_167insCTGA XP_011528072.1:p.Leu56SerfsTer?
XM_017028487.1:c.13_14insCTGA XP_016883976.1:p.Leu5SerfsTer?
XR_937576.2:n.392_393insCTGA
NM_001001890.3:c.85_86insCTGA NP_001001890.1:p.Leu29SerfsTer?
NM_001122607.2:c.85_86insCTGA NP_001116079.1:p.Leu29SerfsTer?
NM_001754.5:c.166_167insCTGA MANE Select NP_001745.2:p.Leu56SerfsTer?