Canonical Allele Identifier: CA2739267615
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2840670
ClinVar RCV Id: RCV003630730

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880547_34880557del , CM000683.2:g.34880547_34880557del GRCh38
NC_000021.8:g.36252844_36252854del , CM000683.1:g.36252844_36252854del GRCh37
NC_000021.7:g.35174714_35174724del NCBI36
NG_011402.2:g.1109155_1109165del , LRG_482:g.1109155_1109165del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.508_508+10del
ENST00000300305.7:c.508_508+10del
ENST00000344691.8:c.427_427+10del
ENST00000358356.9:c.427_427+10del
ENST00000399237.6:c.472_472+10del
ENST00000399240.5:c.427_427+10del
ENST00000437180.5:c.508_508+10del
ENST00000482318.5:c.*98_*98+10del
NM_001001890.2:c.427_427+10del
NM_001122607.1:c.427_427+10del
NM_001754.4:c.508_508+10del , LRG_482t1:c.508_508+10del
XM_005261068.3:c.472_472+10del
XM_005261069.3:c.508_508+10del
XM_011529766.1:c.508_508+10del
XM_011529767.1:c.469_469+10del
XM_011529768.1:c.469_469+10del
XM_011529770.1:c.508_508+10del
XR_937576.1:n.687_687+10del
XM_005261069.4:c.508_508+10del
XM_011529766.2:c.508_508+10del
XM_011529767.2:c.469_469+10del
XM_011529768.2:c.469_469+10del
XM_011529770.2:c.508_508+10del
XM_017028487.1:c.355_355+10del
XR_937576.2:n.734_734+10del
NM_001001890.3:c.427_427+10del
NM_001122607.2:c.427_427+10del
NM_001754.5:c.508_508+10del