Canonical Allele Identifier: CA891842367
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880557_34880563dup , CM000683.2:g.34880557_34880563dup GRCh38
NC_000021.8:g.36252854_36252860dup , CM000683.1:g.36252854_36252860dup GRCh37
NC_000021.7:g.35174724_35174730dup NCBI36
NG_011402.2:g.1109150_1109156dup , LRG_482:g.1109150_1109156dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.503_508+1dup
ENST00000300305.7:c.503_508+1dup
ENST00000344691.8:c.422_427+1dup
ENST00000358356.9:c.422_427+1dup
ENST00000399237.6:c.467_472+1dup
ENST00000399240.5:c.422_427+1dup
ENST00000437180.5:c.503_508+1dup
ENST00000482318.5:c.*93_*98+1dup
NM_001001890.2:c.422_427+1dup
NM_001122607.1:c.422_427+1dup
NM_001754.4:c.503_508+1dup , LRG_482t1:c.503_508+1dup
XM_005261068.3:c.467_472+1dup
XM_005261069.3:c.503_508+1dup
XM_011529766.1:c.503_508+1dup
XM_011529767.1:c.464_469+1dup
XM_011529768.1:c.464_469+1dup
XM_011529770.1:c.503_508+1dup
XR_937576.1:n.682_687+1dup
XM_005261069.4:c.503_508+1dup
XM_011529766.2:c.503_508+1dup
XM_011529767.2:c.464_469+1dup
XM_011529768.2:c.464_469+1dup
XM_011529770.2:c.503_508+1dup
XM_017028487.1:c.350_355+1dup
XR_937576.2:n.729_734+1dup
NM_001001890.3:c.422_427+1dup
NM_001122607.2:c.422_427+1dup
NM_001754.5:c.503_508+1dup