Canonical Allele Identifier: CA2573051253
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880695_34880696insGGGAT , CM000683.2:g.34880695_34880696insGGGAT GRCh38
NC_000021.8:g.36252992_36252993insGGGAT , CM000683.1:g.36252992_36252993insGGGAT GRCh37
NC_000021.7:g.35174862_35174863insGGGAT NCBI36
NG_011402.2:g.1109016_1109017insATCCC , LRG_482:g.1109016_1109017insATCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.369_370insATCCC MANE Select ENSP00000501943.1:p.Val124IlefsTer11
ENST00000300305.7:c.369_370insATCCC ENSP00000300305.3:p.Val124IlefsTer11
ENST00000344691.8:c.288_289insATCCC ENSP00000340690.4:p.Val97IlefsTer11
ENST00000358356.9:c.288_289insATCCC ENSP00000351123.5:p.Val97IlefsTer11
ENST00000399237.6:c.333_334insATCCC ENSP00000382182.2:p.Val112IlefsTer11
ENST00000399240.5:c.288_289insATCCC ENSP00000382184.1:p.Val97IlefsTer11
ENST00000437180.5:c.369_370insATCCC ENSP00000409227.1:p.Val124IlefsTer11
ENST00000455571.5:c.330_331insATCCC ENSP00000388189.1:p.Val111IlefsTer11
ENST00000482318.5:c.76_77insATCCC ENSP00000477067.1:p.Cys26TyrfsTer?
NM_001001890.2:c.288_289insATCCC NP_001001890.1:p.Val97IlefsTer11
NM_001122607.1:c.288_289insATCCC NP_001116079.1:p.Val97IlefsTer11
NM_001754.4:c.369_370insATCCC , LRG_482t1:c.369_370insATCCC NP_001745.2:p.Val124IlefsTer11
XM_005261068.3:c.333_334insATCCC XP_005261125.1:p.Val112IlefsTer11
XM_005261069.3:c.369_370insATCCC XP_005261126.1:p.Val124IlefsTer11
XM_011529766.1:c.369_370insATCCC XP_011528068.1:p.Val124IlefsTer11
XM_011529767.1:c.330_331insATCCC XP_011528069.1:p.Val111IlefsTer11
XM_011529768.1:c.330_331insATCCC XP_011528070.1:p.Val111IlefsTer11
XM_011529770.1:c.369_370insATCCC XP_011528072.1:p.Val124IlefsTer11
XR_937576.1:n.548_549insATCCC
XM_005261069.4:c.369_370insATCCC XP_005261126.1:p.Val124IlefsTer11
XM_011529766.2:c.369_370insATCCC XP_011528068.1:p.Val124IlefsTer11
XM_011529767.2:c.330_331insATCCC XP_011528069.1:p.Val111IlefsTer11
XM_011529768.2:c.330_331insATCCC XP_011528070.1:p.Val111IlefsTer11
XM_011529770.2:c.369_370insATCCC XP_011528072.1:p.Val124IlefsTer11
XM_017028487.1:c.216_217insATCCC XP_016883976.1:p.Val73IlefsTer11
XR_937576.2:n.595_596insATCCC
NM_001001890.3:c.288_289insATCCC NP_001001890.1:p.Val97IlefsTer11
NM_001122607.2:c.288_289insATCCC NP_001116079.1:p.Val97IlefsTer11
NM_001754.5:c.369_370insATCCC MANE Select NP_001745.2:p.Val124IlefsTer11