Canonical Allele Identifier: CA891842363
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880546_34880557del , CM000683.2:g.34880546_34880557del GRCh38
NC_000021.8:g.36252843_36252854del , CM000683.1:g.36252843_36252854del GRCh37
NC_000021.7:g.35174713_35174724del NCBI36
NG_011402.2:g.1109156_1109167del , LRG_482:g.1109156_1109167del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.508+1_508+12del
ENST00000300305.7:c.508+1_508+12del
ENST00000344691.8:c.427+1_427+12del
ENST00000358356.9:c.427+1_427+12del
ENST00000399237.6:c.472+1_472+12del
ENST00000399240.5:c.427+1_427+12del
ENST00000437180.5:c.508+1_508+12del
ENST00000482318.5:c.*98+1_*98+12del
NM_001001890.2:c.427+1_427+12del
NM_001122607.1:c.427+1_427+12del
NM_001754.4:c.508+1_508+12del , LRG_482t1:c.508+1_508+12del
XM_005261068.3:c.472+1_472+12del
XM_005261069.3:c.508+1_508+12del
XM_011529766.1:c.508+1_508+12del
XM_011529767.1:c.469+1_469+12del
XM_011529768.1:c.469+1_469+12del
XM_011529770.1:c.508+1_508+12del
XR_937576.1:n.687+1_687+12del
XM_005261069.4:c.508+1_508+12del
XM_011529766.2:c.508+1_508+12del
XM_011529767.2:c.469+1_469+12del
XM_011529768.2:c.469+1_469+12del
XM_011529770.2:c.508+1_508+12del
XM_017028487.1:c.355+1_355+12del
XR_937576.2:n.734+1_734+12del
NM_001001890.3:c.427+1_427+12del
NM_001122607.2:c.427+1_427+12del
NM_001754.5:c.508+1_508+12del