Canonical Allele Identifier: CA2695202535
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880558_34880572del , CM000683.2:g.34880558_34880572del GRCh38
NC_000021.8:g.36252855_36252869del , CM000683.1:g.36252855_36252869del GRCh37
NC_000021.7:g.35174725_35174739del NCBI36
NG_011402.2:g.1109143_1109157del , LRG_482:g.1109143_1109157del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.496_508+2del
ENST00000300305.7:c.496_508+2del
ENST00000344691.8:c.415_427+2del
ENST00000358356.9:c.415_427+2del
ENST00000399237.6:c.460_472+2del
ENST00000399240.5:c.415_427+2del
ENST00000437180.5:c.496_508+2del
ENST00000482318.5:c.*86_*98+2del
NM_001001890.2:c.415_427+2del
NM_001122607.1:c.415_427+2del
NM_001754.4:c.496_508+2del , LRG_482t1:c.496_508+2del
XM_005261068.3:c.460_472+2del
XM_005261069.3:c.496_508+2del
XM_011529766.1:c.496_508+2del
XM_011529767.1:c.457_469+2del
XM_011529768.1:c.457_469+2del
XM_011529770.1:c.496_508+2del
XR_937576.1:n.675_687+2del
XM_005261069.4:c.496_508+2del
XM_011529766.2:c.496_508+2del
XM_011529767.2:c.457_469+2del
XM_011529768.2:c.457_469+2del
XM_011529770.2:c.496_508+2del
XM_017028487.1:c.343_355+2del
XR_937576.2:n.722_734+2del
NM_001001890.3:c.415_427+2del
NM_001122607.2:c.415_427+2del
NM_001754.5:c.496_508+2del