Canonical Allele Identifier: CA2695202531
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886851dup , CM000683.2:g.34886851dup GRCh38
NC_000021.8:g.36259148dup , CM000683.1:g.36259148dup GRCh37
NC_000021.7:g.35181018dup NCBI36
NG_011402.2:g.1102861dup , LRG_482:g.1102861dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.343dup MANE Select ENSP00000501943.1:p.Ala115GlyfsTer23
ENST00000300305.7:c.343dup ENSP00000300305.3:p.Ala115GlyfsTer23
ENST00000344691.8:c.262dup ENSP00000340690.4:p.Ala88GlyfsTer23
ENST00000358356.9:c.262dup ENSP00000351123.5:p.Ala88GlyfsTer23
ENST00000399237.6:c.307dup ENSP00000382182.2:p.Ala103GlyfsTer23
ENST00000399240.5:c.262dup ENSP00000382184.1:p.Ala88GlyfsTer23
ENST00000437180.5:c.343dup ENSP00000409227.1:p.Ala115GlyfsTer23
ENST00000455571.5:c.304dup ENSP00000388189.1:p.Ala102GlyfsTer23
ENST00000482318.5:c.59-6138dup ENSP00000477067.1:n.59-6138dup
NM_001001890.2:c.262dup NP_001001890.1:p.Ala88GlyfsTer23
NM_001122607.1:c.262dup NP_001116079.1:p.Ala88GlyfsTer23
NM_001754.4:c.343dup , LRG_482t1:c.343dup NP_001745.2:p.Ala115GlyfsTer23
XM_005261068.3:c.307dup XP_005261125.1:p.Ala103GlyfsTer23
XM_005261069.3:c.343dup XP_005261126.1:p.Ala115GlyfsTer23
XM_011529766.1:c.343dup XP_011528068.1:p.Ala115GlyfsTer23
XM_011529767.1:c.304dup XP_011528069.1:p.Ala102GlyfsTer23
XM_011529768.1:c.304dup XP_011528070.1:p.Ala102GlyfsTer23
XM_011529770.1:c.343dup XP_011528072.1:p.Ala115GlyfsTer23
XR_937576.1:n.522dup
XM_005261069.4:c.343dup XP_005261126.1:p.Ala115GlyfsTer23
XM_011529766.2:c.343dup XP_011528068.1:p.Ala115GlyfsTer23
XM_011529767.2:c.304dup XP_011528069.1:p.Ala102GlyfsTer23
XM_011529768.2:c.304dup XP_011528070.1:p.Ala102GlyfsTer23
XM_011529770.2:c.343dup XP_011528072.1:p.Ala115GlyfsTer23
XM_017028487.1:c.190dup XP_016883976.1:p.Ala64GlyfsTer23
XR_937576.2:n.569dup
NM_001001890.3:c.262dup NP_001001890.1:p.Ala88GlyfsTer23
NM_001122607.2:c.262dup NP_001116079.1:p.Ala88GlyfsTer23
NM_001754.5:c.343dup MANE Select NP_001745.2:p.Ala115GlyfsTer23