Canonical Allele Identifier: CA2387292389
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34876268_34876271delinsAAGG , CM000683.2:g.34876268_34876271delinsAAGG GRCh38
NC_000021.8:g.36248565_36248568delinsAAGG , CM000683.1:g.36248565_36248568delinsAAGG GRCh37
NC_000021.7:g.35170435_35170438delinsAAGG NCBI36
NG_011402.2:g.1113441_1113444delinsCCTT , LRG_482:g.1113441_1113444delinsCCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.508+4286_508+4289delinsCCTT MANE Select ENSP00000501943.1:n.508+4286_508+4289delinsCCTT
ENST00000300305.7:c.508+4286_508+4289delinsCCTT ENSP00000300305.3:n.508+4286_508+4289delinsCCTT
ENST00000344691.8:c.427+4286_427+4289delinsCCTT ENSP00000340690.4:n.427+4286_427+4289delinsCCTT
ENST00000358356.9:c.427+4286_427+4289delinsCCTT ENSP00000351123.5:n.427+4286_427+4289delinsCCTT
ENST00000399237.6:c.472+4286_472+4289delinsCCTT ENSP00000382182.2:n.472+4286_472+4289delinsCCTT
ENST00000399240.5:c.427+4286_427+4289delinsCCTT ENSP00000382184.1:n.427+4286_427+4289delinsCCTT
ENST00000437180.5:c.508+4286_508+4289delinsCCTT ENSP00000409227.1:n.508+4286_508+4289delinsCCTT
ENST00000482318.5:c.*98+4286_*98+4289delinsCCTT ENSP00000477067.1:n.*98+4286_*98+4289delinsCCTT
NM_001001890.2:c.427+4286_427+4289delinsCCTT NP_001001890.1:n.427+4286_427+4289delinsCCTT
NM_001122607.1:c.427+4286_427+4289delinsCCTT NP_001116079.1:n.427+4286_427+4289delinsCCTT
NM_001754.4:c.508+4286_508+4289delinsCCTT , LRG_482t1:c.508+4286_508+4289delinsCCTT NP_001745.2:n.508+4286_508+4289delinsCCTT
XM_005261068.3:c.472+4286_472+4289delinsCCTT XP_005261125.1:n.472+4286_472+4289delinsCCTT
XM_005261069.3:c.508+4286_508+4289delinsCCTT XP_005261126.1:n.508+4286_508+4289delinsCCTT
XM_011529766.1:c.508+4286_508+4289delinsCCTT XP_011528068.1:n.508+4286_508+4289delinsCCTT
XM_011529767.1:c.469+4286_469+4289delinsCCTT XP_011528069.1:n.469+4286_469+4289delinsCCTT
XM_011529768.1:c.469+4286_469+4289delinsCCTT XP_011528070.1:n.469+4286_469+4289delinsCCTT
XM_011529770.1:c.508+4286_508+4289delinsCCTT XP_011528072.1:n.508+4286_508+4289delinsCCTT
XR_937576.1:n.687+4286_687+4289delinsCCTT
XM_005261069.4:c.508+4286_508+4289delinsCCTT XP_005261126.1:n.508+4286_508+4289delinsCCTT
XM_011529766.2:c.508+4286_508+4289delinsCCTT XP_011528068.1:n.508+4286_508+4289delinsCCTT
XM_011529767.2:c.469+4286_469+4289delinsCCTT XP_011528069.1:n.469+4286_469+4289delinsCCTT
XM_011529768.2:c.469+4286_469+4289delinsCCTT XP_011528070.1:n.469+4286_469+4289delinsCCTT
XM_011529770.2:c.508+4286_508+4289delinsCCTT XP_011528072.1:n.508+4286_508+4289delinsCCTT
XM_017028487.1:c.355+4286_355+4289delinsCCTT XP_016883976.1:n.355+4286_355+4289delinsCCTT
XR_937576.2:n.734+4286_734+4289delinsCCTT
NM_001001890.3:c.427+4286_427+4289delinsCCTT NP_001001890.1:n.427+4286_427+4289delinsCCTT
NM_001122607.2:c.427+4286_427+4289delinsCCTT NP_001116079.1:n.427+4286_427+4289delinsCCTT
NM_001754.5:c.508+4286_508+4289delinsCCTT MANE Select NP_001745.2:n.508+4286_508+4289delinsCCTT