Canonical Allele Identifier: CA645607431
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886885_34886886dup , CM000683.2:g.34886885_34886886dup GRCh38
NC_000021.8:g.36259182_36259183dup , CM000683.1:g.36259182_36259183dup GRCh37
NC_000021.7:g.35181052_35181053dup NCBI36
NG_011402.2:g.1102826_1102827dup , LRG_482:g.1102826_1102827dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.308_309dup MANE Select ENSP00000501943.1:p.Thr104LeufsTer19
ENST00000300305.7:c.308_309dup ENSP00000300305.3:p.Thr104LeufsTer19
ENST00000344691.8:c.227_228dup ENSP00000340690.4:p.Thr77LeufsTer19
ENST00000358356.9:c.227_228dup ENSP00000351123.5:p.Thr77LeufsTer19
ENST00000399237.6:c.272_273dup ENSP00000382182.2:p.Thr92LeufsTer19
ENST00000399240.5:c.227_228dup ENSP00000382184.1:p.Thr77LeufsTer19
ENST00000437180.5:c.308_309dup ENSP00000409227.1:p.Thr104LeufsTer19
ENST00000455571.5:c.269_270dup ENSP00000388189.1:p.Thr91LeufsTer19
ENST00000482318.5:c.59-6173_59-6172dup ENSP00000477067.1:n.59-6173_59-6172dup
NM_001001890.2:c.227_228dup NP_001001890.1:p.Thr77LeufsTer19
NM_001122607.1:c.227_228dup NP_001116079.1:p.Thr77LeufsTer19
NM_001754.4:c.308_309dup , LRG_482t1:c.308_309dup NP_001745.2:p.Thr104LeufsTer19
XM_005261068.3:c.272_273dup XP_005261125.1:p.Thr92LeufsTer19
XM_005261069.3:c.308_309dup XP_005261126.1:p.Thr104LeufsTer19
XM_011529766.1:c.308_309dup XP_011528068.1:p.Thr104LeufsTer19
XM_011529767.1:c.269_270dup XP_011528069.1:p.Thr91LeufsTer19
XM_011529768.1:c.269_270dup XP_011528070.1:p.Thr91LeufsTer19
XM_011529770.1:c.308_309dup XP_011528072.1:p.Thr104LeufsTer19
XR_937576.1:n.487_488dup
XM_005261069.4:c.308_309dup XP_005261126.1:p.Thr104LeufsTer19
XM_011529766.2:c.308_309dup XP_011528068.1:p.Thr104LeufsTer19
XM_011529767.2:c.269_270dup XP_011528069.1:p.Thr91LeufsTer19
XM_011529768.2:c.269_270dup XP_011528070.1:p.Thr91LeufsTer19
XM_011529770.2:c.308_309dup XP_011528072.1:p.Thr104LeufsTer19
XM_017028487.1:c.155_156dup XP_016883976.1:p.Thr53LeufsTer19
XR_937576.2:n.534_535dup
NM_001001890.3:c.227_228dup NP_001001890.1:p.Thr77LeufsTer19
NM_001122607.2:c.227_228dup NP_001116079.1:p.Thr77LeufsTer19
NM_001754.5:c.308_309dup MANE Select NP_001745.2:p.Thr104LeufsTer19