Canonical Allele Identifier: CA645607336
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880572_34880573insCGGCACC , CM000683.2:g.34880572_34880573insCGGCACC GRCh38
NC_000021.8:g.36252869_36252870insCGGCACC , CM000683.1:g.36252869_36252870insCGGCACC GRCh37
NC_000021.7:g.35174739_35174740insCGGCACC NCBI36
NG_011402.2:g.1109142_1109143insGCCGGGT , LRG_482:g.1109142_1109143insGCCGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.495_496insGCCGGGT MANE Select ENSP00000501943.1:p.Arg166AlafsTer?
ENST00000300305.7:c.495_496insGCCGGGT ENSP00000300305.3:p.Arg166AlafsTer?
ENST00000344691.8:c.414_415insGCCGGGT ENSP00000340690.4:p.Arg139AlafsTer?
ENST00000358356.9:c.414_415insGCCGGGT ENSP00000351123.5:p.Arg139AlafsTer?
ENST00000399237.6:c.459_460insGCCGGGT ENSP00000382182.2:p.Arg154AlafsTer?
ENST00000399240.5:c.414_415insGCCGGGT ENSP00000382184.1:p.Arg139AlafsTer?
ENST00000437180.5:c.495_496insGCCGGGT ENSP00000409227.1:p.Arg166AlafsTer?
ENST00000482318.5:c.*85_*86insGCCGGGT ENSP00000477067.1:n.*85_*86insGCCGGGT
NM_001001890.2:c.414_415insGCCGGGT NP_001001890.1:p.Arg139AlafsTer?
NM_001122607.1:c.414_415insGCCGGGT NP_001116079.1:p.Arg139AlafsTer?
NM_001754.4:c.495_496insGCCGGGT , LRG_482t1:c.495_496insGCCGGGT NP_001745.2:p.Arg166AlafsTer?
XM_005261068.3:c.459_460insGCCGGGT XP_005261125.1:p.Arg154AlafsTer?
XM_005261069.3:c.495_496insGCCGGGT XP_005261126.1:p.Arg166AlafsTer?
XM_011529766.1:c.495_496insGCCGGGT XP_011528068.1:p.Arg166AlafsTer?
XM_011529767.1:c.456_457insGCCGGGT XP_011528069.1:p.Arg153AlafsTer?
XM_011529768.1:c.456_457insGCCGGGT XP_011528070.1:p.Arg153AlafsTer?
XM_011529770.1:c.495_496insGCCGGGT XP_011528072.1:p.Arg166AlafsTer?
XR_937576.1:n.674_675insGCCGGGT
XM_005261069.4:c.495_496insGCCGGGT XP_005261126.1:p.Arg166AlafsTer?
XM_011529766.2:c.495_496insGCCGGGT XP_011528068.1:p.Arg166AlafsTer?
XM_011529767.2:c.456_457insGCCGGGT XP_011528069.1:p.Arg153AlafsTer?
XM_011529768.2:c.456_457insGCCGGGT XP_011528070.1:p.Arg153AlafsTer?
XM_011529770.2:c.495_496insGCCGGGT XP_011528072.1:p.Arg166AlafsTer?
XM_017028487.1:c.342_343insGCCGGGT XP_016883976.1:p.Arg115AlafsTer?
XR_937576.2:n.721_722insGCCGGGT
NM_001001890.3:c.414_415insGCCGGGT NP_001001890.1:p.Arg139AlafsTer?
NM_001122607.2:c.414_415insGCCGGGT NP_001116079.1:p.Arg139AlafsTer?
NM_001754.5:c.495_496insGCCGGGT MANE Select NP_001745.2:p.Arg166AlafsTer?