Canonical Allele Identifier: CA512318902
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886956_34886957insG , CM000683.2:g.34886956_34886957insG GRCh38
NC_000021.8:g.36259253_36259254insG , CM000683.1:g.36259253_36259254insG GRCh37
NC_000021.7:g.35181123_35181124insG NCBI36
NG_011402.2:g.1102755_1102756insC , LRG_482:g.1102755_1102756insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.237_238insC MANE Select ENSP00000501943.1:p.Glu80ArgfsTer?
ENST00000300305.7:c.237_238insC ENSP00000300305.3:p.Glu80ArgfsTer?
ENST00000344691.8:c.156_157insC ENSP00000340690.4:p.Glu53ArgfsTer?
ENST00000358356.9:c.156_157insC ENSP00000351123.5:p.Glu53ArgfsTer?
ENST00000399237.6:c.201_202insC ENSP00000382182.2:p.Glu68ArgfsTer?
ENST00000399240.5:c.156_157insC ENSP00000382184.1:p.Glu53ArgfsTer?
ENST00000437180.5:c.237_238insC ENSP00000409227.1:p.Glu80ArgfsTer?
ENST00000455571.5:c.198_199insC ENSP00000388189.1:p.Glu67ArgfsTer?
ENST00000482318.5:c.59-6244_59-6243insC ENSP00000477067.1:n.59-6244_59-6243insC
NM_001001890.2:c.156_157insC NP_001001890.1:p.Glu53ArgfsTer?
NM_001122607.1:c.156_157insC NP_001116079.1:p.Glu53ArgfsTer?
NM_001754.4:c.237_238insC , LRG_482t1:c.237_238insC NP_001745.2:p.Glu80ArgfsTer?
XM_005261068.3:c.201_202insC XP_005261125.1:p.Glu68ArgfsTer?
XM_005261069.3:c.237_238insC XP_005261126.1:p.Glu80ArgfsTer?
XM_011529766.1:c.237_238insC XP_011528068.1:p.Glu80ArgfsTer?
XM_011529767.1:c.198_199insC XP_011528069.1:p.Glu67ArgfsTer?
XM_011529768.1:c.198_199insC XP_011528070.1:p.Glu67ArgfsTer?
XM_011529770.1:c.237_238insC XP_011528072.1:p.Glu80ArgfsTer?
XR_937576.1:n.416_417insC
XM_005261069.4:c.237_238insC XP_005261126.1:p.Glu80ArgfsTer?
XM_011529766.2:c.237_238insC XP_011528068.1:p.Glu80ArgfsTer?
XM_011529767.2:c.198_199insC XP_011528069.1:p.Glu67ArgfsTer?
XM_011529768.2:c.198_199insC XP_011528070.1:p.Glu67ArgfsTer?
XM_011529770.2:c.237_238insC XP_011528072.1:p.Glu80ArgfsTer?
XM_017028487.1:c.84_85insC XP_016883976.1:p.Glu29ArgfsTer?
XR_937576.2:n.463_464insC
NM_001001890.3:c.156_157insC NP_001001890.1:p.Glu53ArgfsTer?
NM_001122607.2:c.156_157insC NP_001116079.1:p.Glu53ArgfsTer?
NM_001754.5:c.237_238insC MANE Select NP_001745.2:p.Glu80ArgfsTer?