Canonical Allele Identifier: CA2654380330
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887112del , CM000683.2:g.34887112del GRCh38
NC_000021.8:g.36259409del , CM000683.1:g.36259409del GRCh37
NC_000021.7:g.35181279del NCBI36
NG_011402.2:g.1102600del , LRG_482:g.1102600del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.98-16del MANE Select ENSP00000501943.1:n.98-16del
ENST00000300305.7:c.98-16del ENSP00000300305.3:n.98-16del
ENST00000344691.8:c.1del ENSP00000340690.4:p.Met1CysfsTer5
ENST00000358356.9:c.1del ENSP00000351123.5:p.Met1CysfsTer5
ENST00000399237.6:c.62-16del ENSP00000382182.2:n.62-16del
ENST00000399240.5:c.1del ENSP00000382184.1:p.Met1CysfsTer5
ENST00000437180.5:c.98-16del ENSP00000409227.1:n.98-16del
ENST00000455571.5:c.59-16del ENSP00000388189.1:n.59-16del
ENST00000475045.6:c.98-16del ENSP00000477072.1:n.98-16del
ENST00000482318.5:c.59-6399del ENSP00000477067.1:n.59-6399del
NM_001001890.2:c.1del NP_001001890.1:p.Met1CysfsTer5
NM_001122607.1:c.1del NP_001116079.1:p.Met1CysfsTer5
NM_001754.4:c.98-16del , LRG_482t1:c.98-16del NP_001745.2:n.98-16del
XM_005261068.3:c.62-16del XP_005261125.1:n.62-16del
XM_005261069.3:c.98-16del XP_005261126.1:n.98-16del
XM_011529766.1:c.98-16del XP_011528068.1:n.98-16del
XM_011529767.1:c.59-16del XP_011528069.1:n.59-16del
XM_011529768.1:c.59-16del XP_011528070.1:n.59-16del
XM_011529770.1:c.98-16del XP_011528072.1:n.98-16del
XR_937576.1:n.277-16del
XM_005261069.4:c.98-16del XP_005261126.1:n.98-16del
XM_011529766.2:c.98-16del XP_011528068.1:n.98-16del
XM_011529767.2:c.59-16del XP_011528069.1:n.59-16del
XM_011529768.2:c.59-16del XP_011528070.1:n.59-16del
XM_011529770.2:c.98-16del XP_011528072.1:n.98-16del
XM_017028487.1:c.-56-16del XP_016883976.1:n.-56-16del
XR_937576.2:n.324-16del
NM_001001890.3:c.1del NP_001001890.1:p.Met1CysfsTer5
NM_001122607.2:c.1del NP_001116079.1:p.Met1CysfsTer5
NM_001754.5:c.98-16del MANE Select NP_001745.2:n.98-16del