Canonical Allele Identifier: CA2387294238
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880409_34880410delinsTA , CM000683.2:g.34880409_34880410delinsTA GRCh38
NC_000021.8:g.36252706_36252707delinsTA , CM000683.1:g.36252706_36252707delinsTA GRCh37
NC_000021.7:g.35174576_35174577delinsTA NCBI36
NG_011402.2:g.1109302_1109303delinsTA , LRG_482:g.1109302_1109303delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.508+147_508+148delinsTA MANE Select ENSP00000501943.1:n.508+147_508+148delinsTA
ENST00000300305.7:c.508+147_508+148delinsTA ENSP00000300305.3:n.508+147_508+148delinsTA
ENST00000344691.8:c.427+147_427+148delinsTA ENSP00000340690.4:n.427+147_427+148delinsTA
ENST00000358356.9:c.427+147_427+148delinsTA ENSP00000351123.5:n.427+147_427+148delinsTA
ENST00000399237.6:c.472+147_472+148delinsTA ENSP00000382182.2:n.472+147_472+148delinsTA
ENST00000399240.5:c.427+147_427+148delinsTA ENSP00000382184.1:n.427+147_427+148delinsTA
ENST00000437180.5:c.508+147_508+148delinsTA ENSP00000409227.1:n.508+147_508+148delinsTA
ENST00000482318.5:c.*98+147_*98+148delinsTA ENSP00000477067.1:n.*98+147_*98+148delinsTA
NM_001001890.2:c.427+147_427+148delinsTA NP_001001890.1:n.427+147_427+148delinsTA
NM_001122607.1:c.427+147_427+148delinsTA NP_001116079.1:n.427+147_427+148delinsTA
NM_001754.4:c.508+147_508+148delinsTA , LRG_482t1:c.508+147_508+148delinsTA NP_001745.2:n.508+147_508+148delinsTA
XM_005261068.3:c.472+147_472+148delinsTA XP_005261125.1:n.472+147_472+148delinsTA
XM_005261069.3:c.508+147_508+148delinsTA XP_005261126.1:n.508+147_508+148delinsTA
XM_011529766.1:c.508+147_508+148delinsTA XP_011528068.1:n.508+147_508+148delinsTA
XM_011529767.1:c.469+147_469+148delinsTA XP_011528069.1:n.469+147_469+148delinsTA
XM_011529768.1:c.469+147_469+148delinsTA XP_011528070.1:n.469+147_469+148delinsTA
XM_011529770.1:c.508+147_508+148delinsTA XP_011528072.1:n.508+147_508+148delinsTA
XR_937576.1:n.687+147_687+148delinsTA
XM_005261069.4:c.508+147_508+148delinsTA XP_005261126.1:n.508+147_508+148delinsTA
XM_011529766.2:c.508+147_508+148delinsTA XP_011528068.1:n.508+147_508+148delinsTA
XM_011529767.2:c.469+147_469+148delinsTA XP_011528069.1:n.469+147_469+148delinsTA
XM_011529768.2:c.469+147_469+148delinsTA XP_011528070.1:n.469+147_469+148delinsTA
XM_011529770.2:c.508+147_508+148delinsTA XP_011528072.1:n.508+147_508+148delinsTA
XM_017028487.1:c.355+147_355+148delinsTA XP_016883976.1:n.355+147_355+148delinsTA
XR_937576.2:n.734+147_734+148delinsTA
NM_001001890.3:c.427+147_427+148delinsTA NP_001001890.1:n.427+147_427+148delinsTA
NM_001122607.2:c.427+147_427+148delinsTA NP_001116079.1:n.427+147_427+148delinsTA
NM_001754.5:c.508+147_508+148delinsTA MANE Select NP_001745.2:n.508+147_508+148delinsTA