Canonical Allele Identifier: CA2387294207
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs2057877873
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880355del , CM000683.2:g.34880355del GRCh38
NC_000021.8:g.36252652del , CM000683.1:g.36252652del GRCh37
NC_000021.7:g.35174522del NCBI36
NG_011402.2:g.1109357del , LRG_482:g.1109357del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.508+202del MANE Select ENSP00000501943.1:n.508+202del
ENST00000300305.7:c.508+202del ENSP00000300305.3:n.508+202del
ENST00000344691.8:c.427+202del ENSP00000340690.4:n.427+202del
ENST00000358356.9:c.427+202del ENSP00000351123.5:n.427+202del
ENST00000399237.6:c.472+202del ENSP00000382182.2:n.472+202del
ENST00000399240.5:c.427+202del ENSP00000382184.1:n.427+202del
ENST00000437180.5:c.508+202del ENSP00000409227.1:n.508+202del
ENST00000482318.5:c.*98+202del ENSP00000477067.1:n.*98+202del
NM_001001890.2:c.427+202del NP_001001890.1:n.427+202del
NM_001122607.1:c.427+202del NP_001116079.1:n.427+202del
NM_001754.4:c.508+202del , LRG_482t1:c.508+202del NP_001745.2:n.508+202del
XM_005261068.3:c.472+202del XP_005261125.1:n.472+202del
XM_005261069.3:c.508+202del XP_005261126.1:n.508+202del
XM_011529766.1:c.508+202del XP_011528068.1:n.508+202del
XM_011529767.1:c.469+202del XP_011528069.1:n.469+202del
XM_011529768.1:c.469+202del XP_011528070.1:n.469+202del
XM_011529770.1:c.508+202del XP_011528072.1:n.508+202del
XR_937576.1:n.687+202del
XM_005261069.4:c.508+202del XP_005261126.1:n.508+202del
XM_011529766.2:c.508+202del XP_011528068.1:n.508+202del
XM_011529767.2:c.469+202del XP_011528069.1:n.469+202del
XM_011529768.2:c.469+202del XP_011528070.1:n.469+202del
XM_011529770.2:c.508+202del XP_011528072.1:n.508+202del
XM_017028487.1:c.355+202del XP_016883976.1:n.355+202del
XR_937576.2:n.734+202del
NM_001001890.3:c.427+202del NP_001001890.1:n.427+202del
NM_001122607.2:c.427+202del NP_001116079.1:n.427+202del
NM_001754.5:c.508+202del MANE Select NP_001745.2:n.508+202del
Search 100 bp 5'
Search 100 bp 3'