Canonical Allele Identifier: CA645607355
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880609del , CM000683.2:g.34880609del GRCh38
NC_000021.8:g.36252906del , CM000683.1:g.36252906del GRCh37
NC_000021.7:g.35174776del NCBI36
NG_011402.2:g.1109103del , LRG_482:g.1109103del

Transcript Alleles

HGVS Amino-acid change
ENST00000675419.1:c.456del MANE Select ENSP00000501943.1:p.Asn153ThrfsTer23
ENST00000300305.7:c.456del ENSP00000300305.3:p.Asn153ThrfsTer23
ENST00000344691.8:c.375del ENSP00000340690.4:p.Asn126ThrfsTer23
ENST00000358356.9:c.375del ENSP00000351123.5:p.Asn126ThrfsTer23
ENST00000399237.6:c.420del ENSP00000382182.2:p.Asn141ThrfsTer23
ENST00000399240.5:c.375del ENSP00000382184.1:p.Asn126ThrfsTer23
ENST00000437180.5:c.456del ENSP00000409227.1:p.Asn153ThrfsTer23
ENST00000455571.5:c.417del ENSP00000388189.1:p.Lys139=
ENST00000482318.5:c.*46del ENSP00000477067.1:n.*46del
NM_001001890.2:c.375del NP_001001890.1:p.Asn126ThrfsTer23
NM_001122607.1:c.375del NP_001116079.1:p.Asn126ThrfsTer23
NM_001754.4:c.456del , LRG_482t1:c.456del NP_001745.2:p.Asn153ThrfsTer23
XM_005261068.3:c.420del XP_005261125.1:p.Asn141ThrfsTer23
XM_005261069.3:c.456del XP_005261126.1:p.Asn153ThrfsTer23
XM_011529766.1:c.456del XP_011528068.1:p.Asn153ThrfsTer23
XM_011529767.1:c.417del XP_011528069.1:p.Asn140ThrfsTer23
XM_011529768.1:c.417del XP_011528070.1:p.Asn140ThrfsTer23
XM_011529770.1:c.456del XP_011528072.1:p.Asn153ThrfsTer23
XR_937576.1:n.635del
XM_005261069.4:c.456del XP_005261126.1:p.Asn153ThrfsTer23
XM_011529766.2:c.456del XP_011528068.1:p.Asn153ThrfsTer23
XM_011529767.2:c.417del XP_011528069.1:p.Asn140ThrfsTer23
XM_011529768.2:c.417del XP_011528070.1:p.Asn140ThrfsTer23
XM_011529770.2:c.456del XP_011528072.1:p.Asn153ThrfsTer23
XM_017028487.1:c.303del XP_016883976.1:p.Asn102ThrfsTer23
XR_937576.2:n.682del
NM_001001890.3:c.375del NP_001001890.1:p.Asn126ThrfsTer23
NM_001122607.2:c.375del NP_001116079.1:p.Asn126ThrfsTer23
NM_001754.5:c.456del MANE Select NP_001745.2:p.Asn153ThrfsTer23