Canonical Allele Identifier: CA2387297137
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886901_34886902delinsAG , CM000683.2:g.34886901_34886902delinsAG GRCh38
NC_000021.8:g.36259198_36259199delinsAG , CM000683.1:g.36259198_36259199delinsAG GRCh37
NC_000021.7:g.35181068_35181069delinsAG NCBI36
NG_011402.2:g.1102810_1102811delinsCT , LRG_482:g.1102810_1102811delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.292_293delinsCT MANE Select ENSP00000501943.1:p.Leu98=
ENST00000300305.7:c.292_293delinsCT ENSP00000300305.3:p.Leu98=
ENST00000344691.8:c.211_212delinsCT ENSP00000340690.4:p.Leu71=
ENST00000358356.9:c.211_212delinsCT ENSP00000351123.5:p.Leu71=
ENST00000399237.6:c.256_257delinsCT ENSP00000382182.2:p.Leu86=
ENST00000399240.5:c.211_212delinsCT ENSP00000382184.1:p.Leu71=
ENST00000437180.5:c.292_293delinsCT ENSP00000409227.1:p.Leu98=
ENST00000455571.5:c.253_254delinsCT ENSP00000388189.1:p.Leu85=
ENST00000482318.5:c.59-6189_59-6188delinsCT ENSP00000477067.1:n.59-6189_59-6188delinsCT
NM_001001890.2:c.211_212delinsCT NP_001001890.1:p.Leu71=
NM_001122607.1:c.211_212delinsCT NP_001116079.1:p.Leu71=
NM_001754.4:c.292_293delinsCT , LRG_482t1:c.292_293delinsCT NP_001745.2:p.Leu98=
XM_005261068.3:c.256_257delinsCT XP_005261125.1:p.Leu86=
XM_005261069.3:c.292_293delinsCT XP_005261126.1:p.Leu98=
XM_011529766.1:c.292_293delinsCT XP_011528068.1:p.Leu98=
XM_011529767.1:c.253_254delinsCT XP_011528069.1:p.Leu85=
XM_011529768.1:c.253_254delinsCT XP_011528070.1:p.Leu85=
XM_011529770.1:c.292_293delinsCT XP_011528072.1:p.Leu98=
XR_937576.1:n.471_472delinsCT
XM_005261069.4:c.292_293delinsCT XP_005261126.1:p.Leu98=
XM_011529766.2:c.292_293delinsCT XP_011528068.1:p.Leu98=
XM_011529767.2:c.253_254delinsCT XP_011528069.1:p.Leu85=
XM_011529768.2:c.253_254delinsCT XP_011528070.1:p.Leu85=
XM_011529770.2:c.292_293delinsCT XP_011528072.1:p.Leu98=
XM_017028487.1:c.139_140delinsCT XP_016883976.1:p.Leu47=
XR_937576.2:n.518_519delinsCT
NM_001001890.3:c.211_212delinsCT NP_001001890.1:p.Leu71=
NM_001122607.2:c.211_212delinsCT NP_001116079.1:p.Leu71=
NM_001754.5:c.292_293delinsCT MANE Select NP_001745.2:p.Leu98=