Canonical Allele Identifier: CA916079769
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880553_34880559dup , CM000683.2:g.34880553_34880559dup GRCh38
NC_000021.8:g.36252850_36252856dup , CM000683.1:g.36252850_36252856dup GRCh37
NC_000021.7:g.35174720_35174726dup NCBI36
NG_011402.2:g.1109154_1109160dup , LRG_482:g.1109154_1109160dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.507_508+5dup
ENST00000300305.7:c.507_508+5dup
ENST00000344691.8:c.426_427+5dup
ENST00000358356.9:c.426_427+5dup
ENST00000399237.6:c.471_472+5dup
ENST00000399240.5:c.426_427+5dup
ENST00000437180.5:c.507_508+5dup
ENST00000482318.5:c.*97_*98+5dup
NM_001001890.2:c.426_427+5dup
NM_001122607.1:c.426_427+5dup
NM_001754.4:c.507_508+5dup , LRG_482t1:c.507_508+5dup
XM_005261068.3:c.471_472+5dup
XM_005261069.3:c.507_508+5dup
XM_011529766.1:c.507_508+5dup
XM_011529767.1:c.468_469+5dup
XM_011529768.1:c.468_469+5dup
XM_011529770.1:c.507_508+5dup
XR_937576.1:n.686_687+5dup
XM_005261069.4:c.507_508+5dup
XM_011529766.2:c.507_508+5dup
XM_011529767.2:c.468_469+5dup
XM_011529768.2:c.468_469+5dup
XM_011529770.2:c.507_508+5dup
XM_017028487.1:c.354_355+5dup
XR_937576.2:n.733_734+5dup
NM_001001890.3:c.426_427+5dup
NM_001122607.2:c.426_427+5dup
NM_001754.5:c.507_508+5dup