Canonical Allele Identifier: CA512318973
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2121544
ClinVar RCV Id: RCV003049215
dbSNP Id: rs1378434360

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887059G>A , CM000683.2:g.34887059G>A GRCh38
NC_000021.8:g.36259356G>A , CM000683.1:g.36259356G>A GRCh37
NC_000021.7:g.35181226G>A NCBI36
NG_011402.2:g.1102653C>T , LRG_482:g.1102653C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.135C>T MANE Select ENSP00000501943.1:p.Thr45=
ENST00000300305.7:c.135C>T ENSP00000300305.3:p.Thr45=
ENST00000344691.8:c.54C>T ENSP00000340690.4:p.Thr18=
ENST00000358356.9:c.54C>T ENSP00000351123.5:p.Thr18=
ENST00000399237.6:c.99C>T ENSP00000382182.2:p.Thr33=
ENST00000399240.5:c.54C>T ENSP00000382184.1:p.Thr18=
ENST00000437180.5:c.135C>T ENSP00000409227.1:p.Thr45=
ENST00000455571.5:c.96C>T ENSP00000388189.1:p.Thr32=
ENST00000475045.6:c.135C>T ENSP00000477072.1:p.Thr45=
ENST00000482318.5:c.59-6346C>T ENSP00000477067.1:n.59-6346C>T
NM_001001890.2:c.54C>T NP_001001890.1:p.Thr18=
NM_001122607.1:c.54C>T NP_001116079.1:p.Thr18=
NM_001754.4:c.135C>T , LRG_482t1:c.135C>T NP_001745.2:p.Thr45=
XM_005261068.3:c.99C>T XP_005261125.1:p.Thr33=
XM_005261069.3:c.135C>T XP_005261126.1:p.Thr45=
XM_011529766.1:c.135C>T XP_011528068.1:p.Thr45=
XM_011529767.1:c.96C>T XP_011528069.1:p.Thr32=
XM_011529768.1:c.96C>T XP_011528070.1:p.Thr32=
XM_011529770.1:c.135C>T XP_011528072.1:p.Thr45=
XR_937576.1:n.314C>T
XM_005261069.4:c.135C>T XP_005261126.1:p.Thr45=
XM_011529766.2:c.135C>T XP_011528068.1:p.Thr45=
XM_011529767.2:c.96C>T XP_011528069.1:p.Thr32=
XM_011529768.2:c.96C>T XP_011528070.1:p.Thr32=
XM_011529770.2:c.135C>T XP_011528072.1:p.Thr45=
XM_017028487.1:c.-19C>T XP_016883976.1:n.-19C>T
XR_937576.2:n.361C>T
NM_001001890.3:c.54C>T NP_001001890.1:p.Thr18=
NM_001122607.2:c.54C>T NP_001116079.1:p.Thr18=
NM_001754.5:c.135C>T MANE Select NP_001745.2:p.Thr45=