Canonical Allele Identifier: CA645607328
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM1180475
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880569_34880570insTTGAACG , CM000683.2:g.34880569_34880570insTTGAACG GRCh38
NC_000021.8:g.36252866_36252867insTTGAACG , CM000683.1:g.36252866_36252867insTTGAACG GRCh37
NC_000021.7:g.35174736_35174737insTTGAACG NCBI36
NG_011402.2:g.1109144_1109145insTTCAACG , LRG_482:g.1109144_1109145insTTCAACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.497_498insTTCAACG MANE Select ENSP00000501943.1:p.Gly168ThrfsTer?
ENST00000300305.7:c.497_498insTTCAACG ENSP00000300305.3:p.Gly168ThrfsTer?
ENST00000344691.8:c.416_417insTTCAACG ENSP00000340690.4:p.Gly141ThrfsTer?
ENST00000358356.9:c.416_417insTTCAACG ENSP00000351123.5:p.Gly141ThrfsTer?
ENST00000399237.6:c.461_462insTTCAACG ENSP00000382182.2:p.Gly156ThrfsTer?
ENST00000399240.5:c.416_417insTTCAACG ENSP00000382184.1:p.Gly141ThrfsTer?
ENST00000437180.5:c.497_498insTTCAACG ENSP00000409227.1:p.Gly168ThrfsTer?
ENST00000482318.5:c.*87_*88insTTCAACG ENSP00000477067.1:n.*87_*88insTTCAACG
NM_001001890.2:c.416_417insTTCAACG NP_001001890.1:p.Gly141ThrfsTer?
NM_001122607.1:c.416_417insTTCAACG NP_001116079.1:p.Gly141ThrfsTer?
NM_001754.4:c.497_498insTTCAACG , LRG_482t1:c.497_498insTTCAACG NP_001745.2:p.Gly168ThrfsTer?
XM_005261068.3:c.461_462insTTCAACG XP_005261125.1:p.Gly156ThrfsTer?
XM_005261069.3:c.497_498insTTCAACG XP_005261126.1:p.Gly168ThrfsTer?
XM_011529766.1:c.497_498insTTCAACG XP_011528068.1:p.Gly168ThrfsTer?
XM_011529767.1:c.458_459insTTCAACG XP_011528069.1:p.Gly155ThrfsTer?
XM_011529768.1:c.458_459insTTCAACG XP_011528070.1:p.Gly155ThrfsTer?
XM_011529770.1:c.497_498insTTCAACG XP_011528072.1:p.Gly168ThrfsTer?
XR_937576.1:n.676_677insTTCAACG
XM_005261069.4:c.497_498insTTCAACG XP_005261126.1:p.Gly168ThrfsTer?
XM_011529766.2:c.497_498insTTCAACG XP_011528068.1:p.Gly168ThrfsTer?
XM_011529767.2:c.458_459insTTCAACG XP_011528069.1:p.Gly155ThrfsTer?
XM_011529768.2:c.458_459insTTCAACG XP_011528070.1:p.Gly155ThrfsTer?
XM_011529770.2:c.497_498insTTCAACG XP_011528072.1:p.Gly168ThrfsTer?
XM_017028487.1:c.344_345insTTCAACG XP_016883976.1:p.Gly117ThrfsTer?
XR_937576.2:n.723_724insTTCAACG
NM_001001890.3:c.416_417insTTCAACG NP_001001890.1:p.Gly141ThrfsTer?
NM_001122607.2:c.416_417insTTCAACG NP_001116079.1:p.Gly141ThrfsTer?
NM_001754.5:c.497_498insTTCAACG MANE Select NP_001745.2:p.Gly168ThrfsTer?
Search 100 bp 5'
Search 100 bp 3'