Canonical Allele Identifier: CA2387297114
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886859_34886860delinsAG , CM000683.2:g.34886859_34886860delinsAG GRCh38
NC_000021.8:g.36259156_36259157delinsAG , CM000683.1:g.36259156_36259157delinsAG GRCh37
NC_000021.7:g.35181026_35181027delinsAG NCBI36
NG_011402.2:g.1102852_1102853delinsCT , LRG_482:g.1102852_1102853delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.334_335delinsCT MANE Select ENSP00000501943.1:p.Leu112=
ENST00000300305.7:c.334_335delinsCT ENSP00000300305.3:p.Leu112=
ENST00000344691.8:c.253_254delinsCT ENSP00000340690.4:p.Leu85=
ENST00000358356.9:c.253_254delinsCT ENSP00000351123.5:p.Leu85=
ENST00000399237.6:c.298_299delinsCT ENSP00000382182.2:p.Leu100=
ENST00000399240.5:c.253_254delinsCT ENSP00000382184.1:p.Leu85=
ENST00000437180.5:c.334_335delinsCT ENSP00000409227.1:p.Leu112=
ENST00000455571.5:c.295_296delinsCT ENSP00000388189.1:p.Leu99=
ENST00000482318.5:c.59-6147_59-6146delinsCT ENSP00000477067.1:n.59-6147_59-6146delinsCT
NM_001001890.2:c.253_254delinsCT NP_001001890.1:p.Leu85=
NM_001122607.1:c.253_254delinsCT NP_001116079.1:p.Leu85=
NM_001754.4:c.334_335delinsCT , LRG_482t1:c.334_335delinsCT NP_001745.2:p.Leu112=
XM_005261068.3:c.298_299delinsCT XP_005261125.1:p.Leu100=
XM_005261069.3:c.334_335delinsCT XP_005261126.1:p.Leu112=
XM_011529766.1:c.334_335delinsCT XP_011528068.1:p.Leu112=
XM_011529767.1:c.295_296delinsCT XP_011528069.1:p.Leu99=
XM_011529768.1:c.295_296delinsCT XP_011528070.1:p.Leu99=
XM_011529770.1:c.334_335delinsCT XP_011528072.1:p.Leu112=
XR_937576.1:n.513_514delinsCT
XM_005261069.4:c.334_335delinsCT XP_005261126.1:p.Leu112=
XM_011529766.2:c.334_335delinsCT XP_011528068.1:p.Leu112=
XM_011529767.2:c.295_296delinsCT XP_011528069.1:p.Leu99=
XM_011529768.2:c.295_296delinsCT XP_011528070.1:p.Leu99=
XM_011529770.2:c.334_335delinsCT XP_011528072.1:p.Leu112=
XM_017028487.1:c.181_182delinsCT XP_016883976.1:p.Leu61=
XR_937576.2:n.560_561delinsCT
NM_001001890.3:c.253_254delinsCT NP_001001890.1:p.Leu85=
NM_001122607.2:c.253_254delinsCT NP_001116079.1:p.Leu85=
NM_001754.5:c.334_335delinsCT MANE Select NP_001745.2:p.Leu112=