Canonical Allele Identifier: CA2387294343
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880624A= , CM000683.2:g.34880624A= GRCh38
NC_000021.8:g.36252921A= , CM000683.1:g.36252921A= GRCh37
NC_000021.7:g.35174791A= NCBI36
NG_011402.2:g.1109088T= , LRG_482:g.1109088T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.441T= MANE Select ENSP00000501943.1:p.Ala147=
ENST00000300305.7:c.441T= ENSP00000300305.3:p.Ala147=
ENST00000344691.8:c.360T= ENSP00000340690.4:p.Ala120=
ENST00000358356.9:c.360T= ENSP00000351123.5:p.Ala120=
ENST00000399237.6:c.405T= ENSP00000382182.2:p.Ala135=
ENST00000399240.5:c.360T= ENSP00000382184.1:p.Ala120=
ENST00000437180.5:c.441T= ENSP00000409227.1:p.Ala147=
ENST00000455571.5:c.402T= ENSP00000388189.1:p.Ala134=
ENST00000482318.5:c.*31T= ENSP00000477067.1:n.*31T=
NM_001001890.2:c.360T= NP_001001890.1:p.Ala120=
NM_001122607.1:c.360T= NP_001116079.1:p.Ala120=
NM_001754.4:c.441T= , LRG_482t1:c.441T= NP_001745.2:p.Ala147=
XM_005261068.3:c.405T= XP_005261125.1:p.Ala135=
XM_005261069.3:c.441T= XP_005261126.1:p.Ala147=
XM_011529766.1:c.441T= XP_011528068.1:p.Ala147=
XM_011529767.1:c.402T= XP_011528069.1:p.Ala134=
XM_011529768.1:c.402T= XP_011528070.1:p.Ala134=
XM_011529770.1:c.441T= XP_011528072.1:p.Ala147=
XR_937576.1:n.620T=
XM_005261069.4:c.441T= XP_005261126.1:p.Ala147=
XM_011529766.2:c.441T= XP_011528068.1:p.Ala147=
XM_011529767.2:c.402T= XP_011528069.1:p.Ala134=
XM_011529768.2:c.402T= XP_011528070.1:p.Ala134=
XM_011529770.2:c.441T= XP_011528072.1:p.Ala147=
XM_017028487.1:c.288T= XP_016883976.1:p.Ala96=
XR_937576.2:n.667T=
NM_001001890.3:c.360T= NP_001001890.1:p.Ala120=
NM_001122607.2:c.360T= NP_001116079.1:p.Ala120=
NM_001754.5:c.441T= MANE Select NP_001745.2:p.Ala147=