Canonical Allele Identifier: CA645607348
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM24800

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880579_34880592del , CM000683.2:g.34880579_34880592del GRCh38
NC_000021.8:g.36252876_36252889del , CM000683.1:g.36252876_36252889del GRCh37
NC_000021.7:g.35174746_35174759del NCBI36
NG_011402.2:g.1109122_1109135del , LRG_482:g.1109122_1109135del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.475_488del MANE Select ENSP00000501943.1:p.Asn159CysfsTer?
ENST00000300305.7:c.475_488del ENSP00000300305.3:p.Asn159CysfsTer?
ENST00000344691.8:c.394_407del ENSP00000340690.4:p.Asn132CysfsTer?
ENST00000358356.9:c.394_407del ENSP00000351123.5:p.Asn132CysfsTer?
ENST00000399237.6:c.439_452del ENSP00000382182.2:p.Asn147CysfsTer?
ENST00000399240.5:c.394_407del ENSP00000382184.1:p.Asn132CysfsTer?
ENST00000437180.5:c.475_488del ENSP00000409227.1:p.Asn159CysfsTer?
ENST00000482318.5:c.*65_*78del ENSP00000477067.1:n.*65_*78del
NM_001001890.2:c.394_407del NP_001001890.1:p.Asn132CysfsTer?
NM_001122607.1:c.394_407del NP_001116079.1:p.Asn132CysfsTer?
NM_001754.4:c.475_488del , LRG_482t1:c.475_488del NP_001745.2:p.Asn159CysfsTer?
XM_005261068.3:c.439_452del XP_005261125.1:p.Asn147CysfsTer?
XM_005261069.3:c.475_488del XP_005261126.1:p.Asn159CysfsTer?
XM_011529766.1:c.475_488del XP_011528068.1:p.Asn159CysfsTer?
XM_011529767.1:c.436_449del XP_011528069.1:p.Asn146CysfsTer?
XM_011529768.1:c.436_449del XP_011528070.1:p.Asn146CysfsTer?
XM_011529770.1:c.475_488del XP_011528072.1:p.Asn159CysfsTer?
XR_937576.1:n.654_667del
XM_005261069.4:c.475_488del XP_005261126.1:p.Asn159CysfsTer?
XM_011529766.2:c.475_488del XP_011528068.1:p.Asn159CysfsTer?
XM_011529767.2:c.436_449del XP_011528069.1:p.Asn146CysfsTer?
XM_011529768.2:c.436_449del XP_011528070.1:p.Asn146CysfsTer?
XM_011529770.2:c.475_488del XP_011528072.1:p.Asn159CysfsTer?
XM_017028487.1:c.322_335del XP_016883976.1:p.Asn108CysfsTer?
XR_937576.2:n.701_714del
NM_001001890.3:c.394_407del NP_001001890.1:p.Asn132CysfsTer?
NM_001122607.2:c.394_407del NP_001116079.1:p.Asn132CysfsTer?
NM_001754.5:c.475_488del MANE Select NP_001745.2:p.Asn159CysfsTer?