Canonical Allele Identifier: CA645607326
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880566_34880567insGC , CM000683.2:g.34880566_34880567insGC GRCh38
NC_000021.8:g.36252863_36252864insGC , CM000683.1:g.36252863_36252864insGC GRCh37
NC_000021.7:g.35174733_35174734insGC NCBI36
NG_011402.2:g.1109145_1109146insGC , LRG_482:g.1109145_1109146insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.498_499insGC MANE Select ENSP00000501943.1:p.Ser167AlafsTer10
ENST00000300305.7:c.498_499insGC ENSP00000300305.3:p.Ser167AlafsTer10
ENST00000344691.8:c.417_418insGC ENSP00000340690.4:p.Ser140AlafsTer10
ENST00000358356.9:c.417_418insGC ENSP00000351123.5:p.Ser140AlafsTer10
ENST00000399237.6:c.462_463insGC ENSP00000382182.2:p.Ser155AlafsTer10
ENST00000399240.5:c.417_418insGC ENSP00000382184.1:p.Ser140AlafsTer10
ENST00000437180.5:c.498_499insGC ENSP00000409227.1:p.Ser167AlafsTer10
ENST00000482318.5:c.*88_*89insGC ENSP00000477067.1:n.*88_*89insGC
NM_001001890.2:c.417_418insGC NP_001001890.1:p.Ser140AlafsTer10
NM_001122607.1:c.417_418insGC NP_001116079.1:p.Ser140AlafsTer10
NM_001754.4:c.498_499insGC , LRG_482t1:c.498_499insGC NP_001745.2:p.Ser167AlafsTer10
XM_005261068.3:c.462_463insGC XP_005261125.1:p.Ser155AlafsTer10
XM_005261069.3:c.498_499insGC XP_005261126.1:p.Ser167AlafsTer10
XM_011529766.1:c.498_499insGC XP_011528068.1:p.Ser167AlafsTer10
XM_011529767.1:c.459_460insGC XP_011528069.1:p.Ser154AlafsTer10
XM_011529768.1:c.459_460insGC XP_011528070.1:p.Ser154AlafsTer10
XM_011529770.1:c.498_499insGC XP_011528072.1:p.Ser167AlafsTer10
XR_937576.1:n.677_678insGC
XM_005261069.4:c.498_499insGC XP_005261126.1:p.Ser167AlafsTer10
XM_011529766.2:c.498_499insGC XP_011528068.1:p.Ser167AlafsTer10
XM_011529767.2:c.459_460insGC XP_011528069.1:p.Ser154AlafsTer10
XM_011529768.2:c.459_460insGC XP_011528070.1:p.Ser154AlafsTer10
XM_011529770.2:c.498_499insGC XP_011528072.1:p.Ser167AlafsTer10
XM_017028487.1:c.345_346insGC XP_016883976.1:p.Ser116AlafsTer10
XR_937576.2:n.724_725insGC
NM_001001890.3:c.417_418insGC NP_001001890.1:p.Ser140AlafsTer10
NM_001122607.2:c.417_418insGC NP_001116079.1:p.Ser140AlafsTer10
NM_001754.5:c.498_499insGC MANE Select NP_001745.2:p.Ser167AlafsTer10