Canonical Allele Identifier: CA645607441
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886909_34886910insTTGG , CM000683.2:g.34886909_34886910insTTGG GRCh38
NC_000021.8:g.36259206_36259207insTTGG , CM000683.1:g.36259206_36259207insTTGG GRCh37
NC_000021.7:g.35181076_35181077insTTGG NCBI36
NG_011402.2:g.1102803_1102804insCAAC , LRG_482:g.1102803_1102804insCAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.285_286insCAAC MANE Select ENSP00000501943.1:p.Asn96GlnfsTer?
ENST00000300305.7:c.285_286insCAAC ENSP00000300305.3:p.Asn96GlnfsTer?
ENST00000344691.8:c.204_205insCAAC ENSP00000340690.4:p.Asn69GlnfsTer?
ENST00000358356.9:c.204_205insCAAC ENSP00000351123.5:p.Asn69GlnfsTer?
ENST00000399237.6:c.249_250insCAAC ENSP00000382182.2:p.Asn84GlnfsTer?
ENST00000399240.5:c.204_205insCAAC ENSP00000382184.1:p.Asn69GlnfsTer?
ENST00000437180.5:c.285_286insCAAC ENSP00000409227.1:p.Asn96GlnfsTer?
ENST00000455571.5:c.246_247insCAAC ENSP00000388189.1:p.Asn83GlnfsTer?
ENST00000482318.5:c.59-6196_59-6195insCAAC ENSP00000477067.1:n.59-6196_59-6195insCAAC
NM_001001890.2:c.204_205insCAAC NP_001001890.1:p.Asn69GlnfsTer?
NM_001122607.1:c.204_205insCAAC NP_001116079.1:p.Asn69GlnfsTer?
NM_001754.4:c.285_286insCAAC , LRG_482t1:c.285_286insCAAC NP_001745.2:p.Asn96GlnfsTer?
XM_005261068.3:c.249_250insCAAC XP_005261125.1:p.Asn84GlnfsTer?
XM_005261069.3:c.285_286insCAAC XP_005261126.1:p.Asn96GlnfsTer?
XM_011529766.1:c.285_286insCAAC XP_011528068.1:p.Asn96GlnfsTer?
XM_011529767.1:c.246_247insCAAC XP_011528069.1:p.Asn83GlnfsTer?
XM_011529768.1:c.246_247insCAAC XP_011528070.1:p.Asn83GlnfsTer?
XM_011529770.1:c.285_286insCAAC XP_011528072.1:p.Asn96GlnfsTer?
XR_937576.1:n.464_465insCAAC
XM_005261069.4:c.285_286insCAAC XP_005261126.1:p.Asn96GlnfsTer?
XM_011529766.2:c.285_286insCAAC XP_011528068.1:p.Asn96GlnfsTer?
XM_011529767.2:c.246_247insCAAC XP_011528069.1:p.Asn83GlnfsTer?
XM_011529768.2:c.246_247insCAAC XP_011528070.1:p.Asn83GlnfsTer?
XM_011529770.2:c.285_286insCAAC XP_011528072.1:p.Asn96GlnfsTer?
XM_017028487.1:c.132_133insCAAC XP_016883976.1:p.Asn45GlnfsTer?
XR_937576.2:n.511_512insCAAC
NM_001001890.3:c.204_205insCAAC NP_001001890.1:p.Asn69GlnfsTer?
NM_001122607.2:c.204_205insCAAC NP_001116079.1:p.Asn69GlnfsTer?
NM_001754.5:c.285_286insCAAC MANE Select NP_001745.2:p.Asn96GlnfsTer?