Canonical Allele Identifier: CA2387294311
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880563_34880564delinsCA , CM000683.2:g.34880563_34880564delinsCA GRCh38
NC_000021.8:g.36252860_36252861delinsCA , CM000683.1:g.36252860_36252861delinsCA GRCh37
NC_000021.7:g.35174730_35174731delinsCA NCBI36
NG_011402.2:g.1109148_1109149delinsTG , LRG_482:g.1109148_1109149delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.501_502delinsTG MANE Select ENSP00000501943.1:p.Ser167=
ENST00000300305.7:c.501_502delinsTG ENSP00000300305.3:p.Ser167=
ENST00000344691.8:c.420_421delinsTG ENSP00000340690.4:p.Ser140=
ENST00000358356.9:c.420_421delinsTG ENSP00000351123.5:p.Ser140=
ENST00000399237.6:c.465_466delinsTG ENSP00000382182.2:p.Ser155=
ENST00000399240.5:c.420_421delinsTG ENSP00000382184.1:p.Ser140=
ENST00000437180.5:c.501_502delinsTG ENSP00000409227.1:p.Ser167=
ENST00000482318.5:c.*91_*92delinsTG ENSP00000477067.1:n.*91_*92delinsTG
NM_001001890.2:c.420_421delinsTG NP_001001890.1:p.Ser140=
NM_001122607.1:c.420_421delinsTG NP_001116079.1:p.Ser140=
NM_001754.4:c.501_502delinsTG , LRG_482t1:c.501_502delinsTG NP_001745.2:p.Ser167=
XM_005261068.3:c.465_466delinsTG XP_005261125.1:p.Ser155=
XM_005261069.3:c.501_502delinsTG XP_005261126.1:p.Ser167=
XM_011529766.1:c.501_502delinsTG XP_011528068.1:p.Ser167=
XM_011529767.1:c.462_463delinsTG XP_011528069.1:p.Ser154=
XM_011529768.1:c.462_463delinsTG XP_011528070.1:p.Ser154=
XM_011529770.1:c.501_502delinsTG XP_011528072.1:p.Ser167=
XR_937576.1:n.680_681delinsTG
XM_005261069.4:c.501_502delinsTG XP_005261126.1:p.Ser167=
XM_011529766.2:c.501_502delinsTG XP_011528068.1:p.Ser167=
XM_011529767.2:c.462_463delinsTG XP_011528069.1:p.Ser154=
XM_011529768.2:c.462_463delinsTG XP_011528070.1:p.Ser154=
XM_011529770.2:c.501_502delinsTG XP_011528072.1:p.Ser167=
XM_017028487.1:c.348_349delinsTG XP_016883976.1:p.Ser116=
XR_937576.2:n.727_728delinsTG
NM_001001890.3:c.420_421delinsTG NP_001001890.1:p.Ser140=
NM_001122607.2:c.420_421delinsTG NP_001116079.1:p.Ser140=
NM_001754.5:c.501_502delinsTG MANE Select NP_001745.2:p.Ser167=