Canonical Allele Identifier: CA2695202536
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880618_34880626del , CM000683.2:g.34880618_34880626del GRCh38
NC_000021.8:g.36252915_36252923del , CM000683.1:g.36252915_36252923del GRCh37
NC_000021.7:g.35174785_35174793del NCBI36
NG_011402.2:g.1109088_1109096del , LRG_482:g.1109088_1109096del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.441_449del MANE Select ENSP00000501943.1:p.Thr148_Ala150del
ENST00000300305.7:c.441_449del ENSP00000300305.3:p.Thr148_Ala150del
ENST00000344691.8:c.360_368del ENSP00000340690.4:p.Thr121_Ala123del
ENST00000358356.9:c.360_368del ENSP00000351123.5:p.Thr121_Ala123del
ENST00000399237.6:c.405_413del ENSP00000382182.2:p.Thr136_Ala138del
ENST00000399240.5:c.360_368del ENSP00000382184.1:p.Thr121_Ala123del
ENST00000437180.5:c.441_449del ENSP00000409227.1:p.Thr148_Ala150del
ENST00000455571.5:c.402_410del ENSP00000388189.1:p.Thr135_Ala137del
ENST00000482318.5:c.*31_*39del ENSP00000477067.1:n.*31_*39del
NM_001001890.2:c.360_368del NP_001001890.1:p.Thr121_Ala123del
NM_001122607.1:c.360_368del NP_001116079.1:p.Thr121_Ala123del
NM_001754.4:c.441_449del , LRG_482t1:c.441_449del NP_001745.2:p.Thr148_Ala150del
XM_005261068.3:c.405_413del XP_005261125.1:p.Thr136_Ala138del
XM_005261069.3:c.441_449del XP_005261126.1:p.Thr148_Ala150del
XM_011529766.1:c.441_449del XP_011528068.1:p.Thr148_Ala150del
XM_011529767.1:c.402_410del XP_011528069.1:p.Thr135_Ala137del
XM_011529768.1:c.402_410del XP_011528070.1:p.Thr135_Ala137del
XM_011529770.1:c.441_449del XP_011528072.1:p.Thr148_Ala150del
XR_937576.1:n.620_628del
XM_005261069.4:c.441_449del XP_005261126.1:p.Thr148_Ala150del
XM_011529766.2:c.441_449del XP_011528068.1:p.Thr148_Ala150del
XM_011529767.2:c.402_410del XP_011528069.1:p.Thr135_Ala137del
XM_011529768.2:c.402_410del XP_011528070.1:p.Thr135_Ala137del
XM_011529770.2:c.441_449del XP_011528072.1:p.Thr148_Ala150del
XM_017028487.1:c.288_296del XP_016883976.1:p.Thr97_Ala99del
XR_937576.2:n.667_675del
NM_001001890.3:c.360_368del NP_001001890.1:p.Thr121_Ala123del
NM_001122607.2:c.360_368del NP_001116079.1:p.Thr121_Ala123del
NM_001754.5:c.441_449del MANE Select NP_001745.2:p.Thr148_Ala150del