Canonical Allele Identifier: CA645607401
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880677_34880678insA , CM000683.2:g.34880677_34880678insA GRCh38
NC_000021.8:g.36252974_36252975insA , CM000683.1:g.36252974_36252975insA GRCh37
NC_000021.7:g.35174844_35174845insA NCBI36
NG_011402.2:g.1109034_1109035insT , LRG_482:g.1109034_1109035insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.387_388insT MANE Select ENSP00000501943.1:p.Val130CysfsTer8
ENST00000300305.7:c.387_388insT ENSP00000300305.3:p.Val130CysfsTer8
ENST00000344691.8:c.306_307insT ENSP00000340690.4:p.Val103CysfsTer8
ENST00000358356.9:c.306_307insT ENSP00000351123.5:p.Val103CysfsTer8
ENST00000399237.6:c.351_352insT ENSP00000382182.2:p.Val118CysfsTer8
ENST00000399240.5:c.306_307insT ENSP00000382184.1:p.Val103CysfsTer8
ENST00000437180.5:c.387_388insT ENSP00000409227.1:p.Val130CysfsTer8
ENST00000455571.5:c.348_349insT ENSP00000388189.1:p.Val117CysfsTer8
ENST00000482318.5:c.94_95insT ENSP00000477067.1:p.Gly32ValfsTer4
NM_001001890.2:c.306_307insT NP_001001890.1:p.Val103CysfsTer8
NM_001122607.1:c.306_307insT NP_001116079.1:p.Val103CysfsTer8
NM_001754.4:c.387_388insT , LRG_482t1:c.387_388insT NP_001745.2:p.Val130CysfsTer8
XM_005261068.3:c.351_352insT XP_005261125.1:p.Val118CysfsTer8
XM_005261069.3:c.387_388insT XP_005261126.1:p.Val130CysfsTer8
XM_011529766.1:c.387_388insT XP_011528068.1:p.Val130CysfsTer8
XM_011529767.1:c.348_349insT XP_011528069.1:p.Val117CysfsTer8
XM_011529768.1:c.348_349insT XP_011528070.1:p.Val117CysfsTer8
XM_011529770.1:c.387_388insT XP_011528072.1:p.Val130CysfsTer8
XR_937576.1:n.566_567insT
XM_005261069.4:c.387_388insT XP_005261126.1:p.Val130CysfsTer8
XM_011529766.2:c.387_388insT XP_011528068.1:p.Val130CysfsTer8
XM_011529767.2:c.348_349insT XP_011528069.1:p.Val117CysfsTer8
XM_011529768.2:c.348_349insT XP_011528070.1:p.Val117CysfsTer8
XM_011529770.2:c.387_388insT XP_011528072.1:p.Val130CysfsTer8
XM_017028487.1:c.234_235insT XP_016883976.1:p.Val79CysfsTer8
XR_937576.2:n.613_614insT
NM_001001890.3:c.306_307insT NP_001001890.1:p.Val103CysfsTer8
NM_001122607.2:c.306_307insT NP_001116079.1:p.Val103CysfsTer8
NM_001754.5:c.387_388insT MANE Select NP_001745.2:p.Val130CysfsTer8