Canonical Allele Identifier: CA645607334
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880570_34880571insGCCCCTGA , CM000683.2:g.34880570_34880571insGCCCCTGA GRCh38
NC_000021.8:g.36252867_36252868insGCCCCTGA , CM000683.1:g.36252867_36252868insGCCCCTGA GRCh37
NC_000021.7:g.35174737_35174738insGCCCCTGA NCBI36
NG_011402.2:g.1109143_1109144insAGGGGCTC , LRG_482:g.1109143_1109144insAGGGGCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.496_497insAGGGGCTC MANE Select ENSP00000501943.1:p.Arg166GlnfsTer13
ENST00000300305.7:c.496_497insAGGGGCTC ENSP00000300305.3:p.Arg166GlnfsTer13
ENST00000344691.8:c.415_416insAGGGGCTC ENSP00000340690.4:p.Arg139GlnfsTer13
ENST00000358356.9:c.415_416insAGGGGCTC ENSP00000351123.5:p.Arg139GlnfsTer13
ENST00000399237.6:c.460_461insAGGGGCTC ENSP00000382182.2:p.Arg154GlnfsTer13
ENST00000399240.5:c.415_416insAGGGGCTC ENSP00000382184.1:p.Arg139GlnfsTer13
ENST00000437180.5:c.496_497insAGGGGCTC ENSP00000409227.1:p.Arg166GlnfsTer13
ENST00000482318.5:c.*86_*87insAGGGGCTC ENSP00000477067.1:n.*86_*87insAGGGGCTC
NM_001001890.2:c.415_416insAGGGGCTC NP_001001890.1:p.Arg139GlnfsTer13
NM_001122607.1:c.415_416insAGGGGCTC NP_001116079.1:p.Arg139GlnfsTer13
NM_001754.4:c.496_497insAGGGGCTC , LRG_482t1:c.496_497insAGGGGCTC NP_001745.2:p.Arg166GlnfsTer13
XM_005261068.3:c.460_461insAGGGGCTC XP_005261125.1:p.Arg154GlnfsTer13
XM_005261069.3:c.496_497insAGGGGCTC XP_005261126.1:p.Arg166GlnfsTer13
XM_011529766.1:c.496_497insAGGGGCTC XP_011528068.1:p.Arg166GlnfsTer13
XM_011529767.1:c.457_458insAGGGGCTC XP_011528069.1:p.Arg153GlnfsTer13
XM_011529768.1:c.457_458insAGGGGCTC XP_011528070.1:p.Arg153GlnfsTer13
XM_011529770.1:c.496_497insAGGGGCTC XP_011528072.1:p.Arg166GlnfsTer13
XR_937576.1:n.675_676insAGGGGCTC
XM_005261069.4:c.496_497insAGGGGCTC XP_005261126.1:p.Arg166GlnfsTer13
XM_011529766.2:c.496_497insAGGGGCTC XP_011528068.1:p.Arg166GlnfsTer13
XM_011529767.2:c.457_458insAGGGGCTC XP_011528069.1:p.Arg153GlnfsTer13
XM_011529768.2:c.457_458insAGGGGCTC XP_011528070.1:p.Arg153GlnfsTer13
XM_011529770.2:c.496_497insAGGGGCTC XP_011528072.1:p.Arg166GlnfsTer13
XM_017028487.1:c.343_344insAGGGGCTC XP_016883976.1:p.Arg115GlnfsTer13
XR_937576.2:n.722_723insAGGGGCTC
NM_001001890.3:c.415_416insAGGGGCTC NP_001001890.1:p.Arg139GlnfsTer13
NM_001122607.2:c.415_416insAGGGGCTC NP_001116079.1:p.Arg139GlnfsTer13
NM_001754.5:c.496_497insAGGGGCTC MANE Select NP_001745.2:p.Arg166GlnfsTer13