Canonical Allele Identifier: CA2573157368
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1389496
ClinVar RCV Id: RCV001917374
dbSNP Id: rs2146414026

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887061_34887063del , CM000683.2:g.34887061_34887063del GRCh38
NC_000021.8:g.36259358_36259360del , CM000683.1:g.36259358_36259360del GRCh37
NC_000021.7:g.35181228_35181230del NCBI36
NG_011402.2:g.1102651_1102653del , LRG_482:g.1102651_1102653del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.133_135del MANE Select ENSP00000501943.1:p.Thr45del
ENST00000300305.7:c.133_135del ENSP00000300305.3:p.Thr45del
ENST00000344691.8:c.52_54del ENSP00000340690.4:p.Thr18del
ENST00000358356.9:c.52_54del ENSP00000351123.5:p.Thr18del
ENST00000399237.6:c.97_99del ENSP00000382182.2:p.Thr33del
ENST00000399240.5:c.52_54del ENSP00000382184.1:p.Thr18del
ENST00000437180.5:c.133_135del ENSP00000409227.1:p.Thr45del
ENST00000455571.5:c.94_96del ENSP00000388189.1:p.Thr32del
ENST00000475045.6:c.133_135del ENSP00000477072.1:p.Thr45del
ENST00000482318.5:c.59-6348_59-6346del ENSP00000477067.1:n.59-6348_59-6346del
NM_001001890.2:c.52_54del NP_001001890.1:p.Thr18del
NM_001122607.1:c.52_54del NP_001116079.1:p.Thr18del
NM_001754.4:c.133_135del , LRG_482t1:c.133_135del NP_001745.2:p.Thr45del
XM_005261068.3:c.97_99del XP_005261125.1:p.Thr33del
XM_005261069.3:c.133_135del XP_005261126.1:p.Thr45del
XM_011529766.1:c.133_135del XP_011528068.1:p.Thr45del
XM_011529767.1:c.94_96del XP_011528069.1:p.Thr32del
XM_011529768.1:c.94_96del XP_011528070.1:p.Thr32del
XM_011529770.1:c.133_135del XP_011528072.1:p.Thr45del
XR_937576.1:n.312_314del
XM_005261069.4:c.133_135del XP_005261126.1:p.Thr45del
XM_011529766.2:c.133_135del XP_011528068.1:p.Thr45del
XM_011529767.2:c.94_96del XP_011528069.1:p.Thr32del
XM_011529768.2:c.94_96del XP_011528070.1:p.Thr32del
XM_011529770.2:c.133_135del XP_011528072.1:p.Thr45del
XM_017028487.1:c.-21_-19del XP_016883976.1:n.-21_-19del
XR_937576.2:n.359_361del
NM_001001890.3:c.52_54del NP_001001890.1:p.Thr18del
NM_001122607.2:c.52_54del NP_001116079.1:p.Thr18del
NM_001754.5:c.133_135del MANE Select NP_001745.2:p.Thr45del