Canonical Allele Identifier: CA645607406
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880696_34880699dup , CM000683.2:g.34880696_34880699dup GRCh38
NC_000021.8:g.36252993_36252996dup , CM000683.1:g.36252993_36252996dup GRCh37
NC_000021.7:g.35174863_35174866dup NCBI36
NG_011402.2:g.1109014_1109017dup , LRG_482:g.1109014_1109017dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.367_370dup MANE Select ENSP00000501943.1:p.Val124GlyfsTer15
ENST00000300305.7:c.367_370dup ENSP00000300305.3:p.Val124GlyfsTer15
ENST00000344691.8:c.286_289dup ENSP00000340690.4:p.Val97GlyfsTer15
ENST00000358356.9:c.286_289dup ENSP00000351123.5:p.Val97GlyfsTer15
ENST00000399237.6:c.331_334dup ENSP00000382182.2:p.Val112GlyfsTer15
ENST00000399240.5:c.286_289dup ENSP00000382184.1:p.Val97GlyfsTer15
ENST00000437180.5:c.367_370dup ENSP00000409227.1:p.Val124GlyfsTer15
ENST00000455571.5:c.328_331dup ENSP00000388189.1:p.Val111GlyfsTer15
ENST00000482318.5:c.74_77dup ENSP00000477067.1:p.Cys26TrpfsTer11
NM_001001890.2:c.286_289dup NP_001001890.1:p.Val97GlyfsTer15
NM_001122607.1:c.286_289dup NP_001116079.1:p.Val97GlyfsTer15
NM_001754.4:c.367_370dup , LRG_482t1:c.367_370dup NP_001745.2:p.Val124GlyfsTer15
XM_005261068.3:c.331_334dup XP_005261125.1:p.Val112GlyfsTer15
XM_005261069.3:c.367_370dup XP_005261126.1:p.Val124GlyfsTer15
XM_011529766.1:c.367_370dup XP_011528068.1:p.Val124GlyfsTer15
XM_011529767.1:c.328_331dup XP_011528069.1:p.Val111GlyfsTer15
XM_011529768.1:c.328_331dup XP_011528070.1:p.Val111GlyfsTer15
XM_011529770.1:c.367_370dup XP_011528072.1:p.Val124GlyfsTer15
XR_937576.1:n.546_549dup
XM_005261069.4:c.367_370dup XP_005261126.1:p.Val124GlyfsTer15
XM_011529766.2:c.367_370dup XP_011528068.1:p.Val124GlyfsTer15
XM_011529767.2:c.328_331dup XP_011528069.1:p.Val111GlyfsTer15
XM_011529768.2:c.328_331dup XP_011528070.1:p.Val111GlyfsTer15
XM_011529770.2:c.367_370dup XP_011528072.1:p.Val124GlyfsTer15
XM_017028487.1:c.214_217dup XP_016883976.1:p.Val73GlyfsTer15
XR_937576.2:n.593_596dup
NM_001001890.3:c.286_289dup NP_001001890.1:p.Val97GlyfsTer15
NM_001122607.2:c.286_289dup NP_001116079.1:p.Val97GlyfsTer15
NM_001754.5:c.367_370dup MANE Select NP_001745.2:p.Val124GlyfsTer15