Canonical Allele Identifier: CA512318853
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1088304
dbSNP Id: rs1432236291

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886903G>A , CM000683.2:g.34886903G>A GRCh38
NC_000021.8:g.36259200G>A , CM000683.1:g.36259200G>A GRCh37
NC_000021.7:g.35181070G>A NCBI36
NG_011402.2:g.1102809C>T , LRG_482:g.1102809C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.291C>T MANE Select ENSP00000501943.1:p.Phe97=
ENST00000300305.7:c.291C>T ENSP00000300305.3:p.Phe97=
ENST00000344691.8:c.210C>T ENSP00000340690.4:p.Phe70=
ENST00000358356.9:c.210C>T ENSP00000351123.5:p.Phe70=
ENST00000399237.6:c.255C>T ENSP00000382182.2:p.Phe85=
ENST00000399240.5:c.210C>T ENSP00000382184.1:p.Phe70=
ENST00000437180.5:c.291C>T ENSP00000409227.1:p.Phe97=
ENST00000455571.5:c.252C>T ENSP00000388189.1:p.Phe84=
ENST00000482318.5:c.59-6190C>T ENSP00000477067.1:n.59-6190C>T
NM_001001890.2:c.210C>T NP_001001890.1:p.Phe70=
NM_001122607.1:c.210C>T NP_001116079.1:p.Phe70=
NM_001754.4:c.291C>T , LRG_482t1:c.291C>T NP_001745.2:p.Phe97=
XM_005261068.3:c.255C>T XP_005261125.1:p.Phe85=
XM_005261069.3:c.291C>T XP_005261126.1:p.Phe97=
XM_011529766.1:c.291C>T XP_011528068.1:p.Phe97=
XM_011529767.1:c.252C>T XP_011528069.1:p.Phe84=
XM_011529768.1:c.252C>T XP_011528070.1:p.Phe84=
XM_011529770.1:c.291C>T XP_011528072.1:p.Phe97=
XR_937576.1:n.470C>T
XM_005261069.4:c.291C>T XP_005261126.1:p.Phe97=
XM_011529766.2:c.291C>T XP_011528068.1:p.Phe97=
XM_011529767.2:c.252C>T XP_011528069.1:p.Phe84=
XM_011529768.2:c.252C>T XP_011528070.1:p.Phe84=
XM_011529770.2:c.291C>T XP_011528072.1:p.Phe97=
XM_017028487.1:c.138C>T XP_016883976.1:p.Phe46=
XR_937576.2:n.517C>T
NM_001001890.3:c.210C>T NP_001001890.1:p.Phe70=
NM_001122607.2:c.210C>T NP_001116079.1:p.Phe70=
NM_001754.5:c.291C>T MANE Select NP_001745.2:p.Phe97=