Canonical Allele Identifier: CA2387294322
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880581T= , CM000683.2:g.34880581T= GRCh38
NC_000021.8:g.36252878T= , CM000683.1:g.36252878T= GRCh37
NC_000021.7:g.35174748T= NCBI36
NG_011402.2:g.1109131A= , LRG_482:g.1109131A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.484A= MANE Select ENSP00000501943.1:p.Arg162=
ENST00000300305.7:c.484A= ENSP00000300305.3:p.Arg162=
ENST00000344691.8:c.403A= ENSP00000340690.4:p.Arg135=
ENST00000358356.9:c.403A= ENSP00000351123.5:p.Arg135=
ENST00000399237.6:c.448A= ENSP00000382182.2:p.Arg150=
ENST00000399240.5:c.403A= ENSP00000382184.1:p.Arg135=
ENST00000437180.5:c.484A= ENSP00000409227.1:p.Arg162=
ENST00000482318.5:c.*74A= ENSP00000477067.1:n.*74A=
NM_001001890.2:c.403A= NP_001001890.1:p.Arg135=
NM_001122607.1:c.403A= NP_001116079.1:p.Arg135=
NM_001754.4:c.484A= , LRG_482t1:c.484A= NP_001745.2:p.Arg162=
XM_005261068.3:c.448A= XP_005261125.1:p.Arg150=
XM_005261069.3:c.484A= XP_005261126.1:p.Arg162=
XM_011529766.1:c.484A= XP_011528068.1:p.Arg162=
XM_011529767.1:c.445A= XP_011528069.1:p.Arg149=
XM_011529768.1:c.445A= XP_011528070.1:p.Arg149=
XM_011529770.1:c.484A= XP_011528072.1:p.Arg162=
XR_937576.1:n.663A=
XM_005261069.4:c.484A= XP_005261126.1:p.Arg162=
XM_011529766.2:c.484A= XP_011528068.1:p.Arg162=
XM_011529767.2:c.445A= XP_011528069.1:p.Arg149=
XM_011529768.2:c.445A= XP_011528070.1:p.Arg149=
XM_011529770.2:c.484A= XP_011528072.1:p.Arg162=
XM_017028487.1:c.331A= XP_016883976.1:p.Arg111=
XR_937576.2:n.710A=
NM_001001890.3:c.403A= NP_001001890.1:p.Arg135=
NM_001122607.2:c.403A= NP_001116079.1:p.Arg135=
NM_001754.5:c.484A= MANE Select NP_001745.2:p.Arg162=