Canonical Allele Identifier: CA2387297198
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887004C= , CM000683.2:g.34887004C= GRCh38
NC_000021.8:g.36259301C= , CM000683.1:g.36259301C= GRCh37
NC_000021.7:g.35181171C= NCBI36
NG_011402.2:g.1102708G= , LRG_482:g.1102708G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.190G= MANE Select ENSP00000501943.1:p.Gly64=
ENST00000300305.7:c.190G= ENSP00000300305.3:p.Gly64=
ENST00000344691.8:c.109G= ENSP00000340690.4:p.Gly37=
ENST00000358356.9:c.109G= ENSP00000351123.5:p.Gly37=
ENST00000399237.6:c.154G= ENSP00000382182.2:p.Gly52=
ENST00000399240.5:c.109G= ENSP00000382184.1:p.Gly37=
ENST00000437180.5:c.190G= ENSP00000409227.1:p.Gly64=
ENST00000455571.5:c.151G= ENSP00000388189.1:p.Gly51=
ENST00000482318.5:c.59-6291G= ENSP00000477067.1:n.59-6291G=
NM_001001890.2:c.109G= NP_001001890.1:p.Gly37=
NM_001122607.1:c.109G= NP_001116079.1:p.Gly37=
NM_001754.4:c.190G= , LRG_482t1:c.190G= NP_001745.2:p.Gly64=
XM_005261068.3:c.154G= XP_005261125.1:p.Gly52=
XM_005261069.3:c.190G= XP_005261126.1:p.Gly64=
XM_011529766.1:c.190G= XP_011528068.1:p.Gly64=
XM_011529767.1:c.151G= XP_011528069.1:p.Gly51=
XM_011529768.1:c.151G= XP_011528070.1:p.Gly51=
XM_011529770.1:c.190G= XP_011528072.1:p.Gly64=
XR_937576.1:n.369G=
XM_005261069.4:c.190G= XP_005261126.1:p.Gly64=
XM_011529766.2:c.190G= XP_011528068.1:p.Gly64=
XM_011529767.2:c.151G= XP_011528069.1:p.Gly51=
XM_011529768.2:c.151G= XP_011528070.1:p.Gly51=
XM_011529770.2:c.190G= XP_011528072.1:p.Gly64=
XM_017028487.1:c.37G= XP_016883976.1:p.Gly13=
XR_937576.2:n.416G=
NM_001001890.3:c.109G= NP_001001890.1:p.Gly37=
NM_001122607.2:c.109G= NP_001116079.1:p.Gly37=
NM_001754.5:c.190G= MANE Select NP_001745.2:p.Gly64=