Canonical Allele Identifier: CA645607318
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880563_34880568del , CM000683.2:g.34880563_34880568del GRCh38
NC_000021.8:g.36252860_36252865del , CM000683.1:g.36252860_36252865del GRCh37
NC_000021.7:g.35174730_35174735del NCBI36
NG_011402.2:g.1109148_1109153del , LRG_482:g.1109148_1109153del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.501_506del MANE Select ENSP00000501943.1:p.Ser167_Gly168del
ENST00000300305.7:c.501_506del ENSP00000300305.3:p.Ser167_Gly168del
ENST00000344691.8:c.420_425del ENSP00000340690.4:p.Ser140_Gly141del
ENST00000358356.9:c.420_425del ENSP00000351123.5:p.Ser140_Gly141del
ENST00000399237.6:c.465_470del ENSP00000382182.2:p.Ser155_Gly156del
ENST00000399240.5:c.420_425del ENSP00000382184.1:p.Ser140_Gly141del
ENST00000437180.5:c.501_506del ENSP00000409227.1:p.Ser167_Gly168del
ENST00000482318.5:c.*91_*96del ENSP00000477067.1:n.*91_*96del
NM_001001890.2:c.420_425del NP_001001890.1:p.Ser140_Gly141del
NM_001122607.1:c.420_425del NP_001116079.1:p.Ser140_Gly141del
NM_001754.4:c.501_506del , LRG_482t1:c.501_506del NP_001745.2:p.Ser167_Gly168del
XM_005261068.3:c.465_470del XP_005261125.1:p.Ser155_Gly156del
XM_005261069.3:c.501_506del XP_005261126.1:p.Ser167_Gly168del
XM_011529766.1:c.501_506del XP_011528068.1:p.Ser167_Gly168del
XM_011529767.1:c.462_467del XP_011528069.1:p.Ser154_Gly155del
XM_011529768.1:c.462_467del XP_011528070.1:p.Ser154_Gly155del
XM_011529770.1:c.501_506del XP_011528072.1:p.Ser167_Gly168del
XR_937576.1:n.680_685del
XM_005261069.4:c.501_506del XP_005261126.1:p.Ser167_Gly168del
XM_011529766.2:c.501_506del XP_011528068.1:p.Ser167_Gly168del
XM_011529767.2:c.462_467del XP_011528069.1:p.Ser154_Gly155del
XM_011529768.2:c.462_467del XP_011528070.1:p.Ser154_Gly155del
XM_011529770.2:c.501_506del XP_011528072.1:p.Ser167_Gly168del
XM_017028487.1:c.348_353del XP_016883976.1:p.Ser116_Gly117del
XR_937576.2:n.727_732del
NM_001001890.3:c.420_425del NP_001001890.1:p.Ser140_Gly141del
NM_001122607.2:c.420_425del NP_001116079.1:p.Ser140_Gly141del
NM_001754.5:c.501_506del MANE Select NP_001745.2:p.Ser167_Gly168del