Canonical Allele Identifier: CA1022023803
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs2057812106

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34876252_34876263del , CM000683.2:g.34876252_34876263del GRCh38
NC_000021.8:g.36248549_36248560del , CM000683.1:g.36248549_36248560del GRCh37
NC_000021.7:g.35170419_35170430del NCBI36
NG_011402.2:g.1113451_1113462del , LRG_482:g.1113451_1113462del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.508+4296_508+4307del MANE Select ENSP00000501943.1:n.508+4296_508+4307del
ENST00000300305.7:c.508+4296_508+4307del ENSP00000300305.3:n.508+4296_508+4307del
ENST00000344691.8:c.427+4296_427+4307del ENSP00000340690.4:n.427+4296_427+4307del
ENST00000358356.9:c.427+4296_427+4307del ENSP00000351123.5:n.427+4296_427+4307del
ENST00000399237.6:c.472+4296_472+4307del ENSP00000382182.2:n.472+4296_472+4307del
ENST00000399240.5:c.427+4296_427+4307del ENSP00000382184.1:n.427+4296_427+4307del
ENST00000437180.5:c.508+4296_508+4307del ENSP00000409227.1:n.508+4296_508+4307del
ENST00000482318.5:c.*98+4296_*98+4307del ENSP00000477067.1:n.*98+4296_*98+4307del
NM_001001890.2:c.427+4296_427+4307del NP_001001890.1:n.427+4296_427+4307del
NM_001122607.1:c.427+4296_427+4307del NP_001116079.1:n.427+4296_427+4307del
NM_001754.4:c.508+4296_508+4307del , LRG_482t1:c.508+4296_508+4307del NP_001745.2:n.508+4296_508+4307del
XM_005261068.3:c.472+4296_472+4307del XP_005261125.1:n.472+4296_472+4307del
XM_005261069.3:c.508+4296_508+4307del XP_005261126.1:n.508+4296_508+4307del
XM_011529766.1:c.508+4296_508+4307del XP_011528068.1:n.508+4296_508+4307del
XM_011529767.1:c.469+4296_469+4307del XP_011528069.1:n.469+4296_469+4307del
XM_011529768.1:c.469+4296_469+4307del XP_011528070.1:n.469+4296_469+4307del
XM_011529770.1:c.508+4296_508+4307del XP_011528072.1:n.508+4296_508+4307del
XR_937576.1:n.687+4296_687+4307del
XM_005261069.4:c.508+4296_508+4307del XP_005261126.1:n.508+4296_508+4307del
XM_011529766.2:c.508+4296_508+4307del XP_011528068.1:n.508+4296_508+4307del
XM_011529767.2:c.469+4296_469+4307del XP_011528069.1:n.469+4296_469+4307del
XM_011529768.2:c.469+4296_469+4307del XP_011528070.1:n.469+4296_469+4307del
XM_011529770.2:c.508+4296_508+4307del XP_011528072.1:n.508+4296_508+4307del
XM_017028487.1:c.355+4296_355+4307del XP_016883976.1:n.355+4296_355+4307del
XR_937576.2:n.734+4296_734+4307del
NM_001001890.3:c.427+4296_427+4307del NP_001001890.1:n.427+4296_427+4307del
NM_001122607.2:c.427+4296_427+4307del NP_001116079.1:n.427+4296_427+4307del
NM_001754.5:c.508+4296_508+4307del MANE Select NP_001745.2:n.508+4296_508+4307del