Canonical Allele Identifier: CA2387297160
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs2058000196

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886946_34886972del , CM000683.2:g.34886946_34886972del GRCh38
NC_000021.8:g.36259243_36259269del , CM000683.1:g.36259243_36259269del GRCh37
NC_000021.7:g.35181113_35181139del NCBI36
NG_011402.2:g.1102745_1102771del , LRG_482:g.1102745_1102771del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.227_253del MANE Select ENSP00000501943.1:p.Arg76_Asp84del
ENST00000300305.7:c.227_253del ENSP00000300305.3:p.Arg76_Asp84del
ENST00000344691.8:c.146_172del ENSP00000340690.4:p.Arg49_Asp57del
ENST00000358356.9:c.146_172del ENSP00000351123.5:p.Arg49_Asp57del
ENST00000399237.6:c.191_217del ENSP00000382182.2:p.Arg64_Asp72del
ENST00000399240.5:c.146_172del ENSP00000382184.1:p.Arg49_Asp57del
ENST00000437180.5:c.227_253del ENSP00000409227.1:p.Arg76_Asp84del
ENST00000455571.5:c.188_214del ENSP00000388189.1:p.Arg63_Asp71del
ENST00000482318.5:c.59-6254_59-6228del ENSP00000477067.1:n.59-6254_59-6228del
NM_001001890.2:c.146_172del NP_001001890.1:p.Arg49_Asp57del
NM_001122607.1:c.146_172del NP_001116079.1:p.Arg49_Asp57del
NM_001754.4:c.227_253del , LRG_482t1:c.227_253del NP_001745.2:p.Arg76_Asp84del
XM_005261068.3:c.191_217del XP_005261125.1:p.Arg64_Asp72del
XM_005261069.3:c.227_253del XP_005261126.1:p.Arg76_Asp84del
XM_011529766.1:c.227_253del XP_011528068.1:p.Arg76_Asp84del
XM_011529767.1:c.188_214del XP_011528069.1:p.Arg63_Asp71del
XM_011529768.1:c.188_214del XP_011528070.1:p.Arg63_Asp71del
XM_011529770.1:c.227_253del XP_011528072.1:p.Arg76_Asp84del
XR_937576.1:n.406_432del
XM_005261069.4:c.227_253del XP_005261126.1:p.Arg76_Asp84del
XM_011529766.2:c.227_253del XP_011528068.1:p.Arg76_Asp84del
XM_011529767.2:c.188_214del XP_011528069.1:p.Arg63_Asp71del
XM_011529768.2:c.188_214del XP_011528070.1:p.Arg63_Asp71del
XM_011529770.2:c.227_253del XP_011528072.1:p.Arg76_Asp84del
XM_017028487.1:c.74_100del XP_016883976.1:p.Arg25_Asp33del
XR_937576.2:n.453_479del
NM_001001890.3:c.146_172del NP_001001890.1:p.Arg49_Asp57del
NM_001122607.2:c.146_172del NP_001116079.1:p.Arg49_Asp57del
NM_001754.5:c.227_253del MANE Select NP_001745.2:p.Arg76_Asp84del