Canonical Allele Identifier: CA891842374
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880667del , CM000683.2:g.34880667del GRCh38
NC_000021.8:g.36252964del , CM000683.1:g.36252964del GRCh37
NC_000021.7:g.35174834del NCBI36
NG_011402.2:g.1109045del , LRG_482:g.1109045del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.398del MANE Select ENSP00000501943.1:p.Met133ArgfsTer12
ENST00000300305.7:c.398del ENSP00000300305.3:p.Met133ArgfsTer12
ENST00000344691.8:c.317del ENSP00000340690.4:p.Met106ArgfsTer12
ENST00000358356.9:c.317del ENSP00000351123.5:p.Met106ArgfsTer12
ENST00000399237.6:c.362del ENSP00000382182.2:p.Met121ArgfsTer12
ENST00000399240.5:c.317del ENSP00000382184.1:p.Met106ArgfsTer12
ENST00000437180.5:c.398del ENSP00000409227.1:p.Met133ArgfsTer12
ENST00000455571.5:c.359del ENSP00000388189.1:p.Met120ArgfsTer12
ENST00000482318.5:c.105del ENSP00000477067.1:p.Asp35GlufsTer?
NM_001001890.2:c.317del NP_001001890.1:p.Met106ArgfsTer12
NM_001122607.1:c.317del NP_001116079.1:p.Met106ArgfsTer12
NM_001754.4:c.398del , LRG_482t1:c.398del NP_001745.2:p.Met133ArgfsTer12
XM_005261068.3:c.362del XP_005261125.1:p.Met121ArgfsTer12
XM_005261069.3:c.398del XP_005261126.1:p.Met133ArgfsTer12
XM_011529766.1:c.398del XP_011528068.1:p.Met133ArgfsTer12
XM_011529767.1:c.359del XP_011528069.1:p.Met120ArgfsTer12
XM_011529768.1:c.359del XP_011528070.1:p.Met120ArgfsTer12
XM_011529770.1:c.398del XP_011528072.1:p.Met133ArgfsTer12
XR_937576.1:n.577del
XM_005261069.4:c.398del XP_005261126.1:p.Met133ArgfsTer12
XM_011529766.2:c.398del XP_011528068.1:p.Met133ArgfsTer12
XM_011529767.2:c.359del XP_011528069.1:p.Met120ArgfsTer12
XM_011529768.2:c.359del XP_011528070.1:p.Met120ArgfsTer12
XM_011529770.2:c.398del XP_011528072.1:p.Met133ArgfsTer12
XM_017028487.1:c.245del XP_016883976.1:p.Met82ArgfsTer12
XR_937576.2:n.624del
NM_001001890.3:c.317del NP_001001890.1:p.Met106ArgfsTer12
NM_001122607.2:c.317del NP_001116079.1:p.Met106ArgfsTer12
NM_001754.5:c.398del MANE Select NP_001745.2:p.Met133ArgfsTer12