Canonical Allele Identifier: CA512318676
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880584_34880585insC , CM000683.2:g.34880584_34880585insC GRCh38
NC_000021.8:g.36252881_36252882insC , CM000683.1:g.36252881_36252882insC GRCh37
NC_000021.7:g.35174751_35174752insC NCBI36
NG_011402.2:g.1109127_1109128insG , LRG_482:g.1109127_1109128insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.480_481insG MANE Select ENSP00000501943.1:p.Leu161AlafsTer?
ENST00000300305.7:c.480_481insG ENSP00000300305.3:p.Leu161AlafsTer?
ENST00000344691.8:c.399_400insG ENSP00000340690.4:p.Leu134AlafsTer?
ENST00000358356.9:c.399_400insG ENSP00000351123.5:p.Leu134AlafsTer?
ENST00000399237.6:c.444_445insG ENSP00000382182.2:p.Leu149AlafsTer?
ENST00000399240.5:c.399_400insG ENSP00000382184.1:p.Leu134AlafsTer?
ENST00000437180.5:c.480_481insG ENSP00000409227.1:p.Leu161AlafsTer?
ENST00000482318.5:c.*70_*71insG ENSP00000477067.1:n.*70_*71insG
NM_001001890.2:c.399_400insG NP_001001890.1:p.Leu134AlafsTer?
NM_001122607.1:c.399_400insG NP_001116079.1:p.Leu134AlafsTer?
NM_001754.4:c.480_481insG , LRG_482t1:c.480_481insG NP_001745.2:p.Leu161AlafsTer?
XM_005261068.3:c.444_445insG XP_005261125.1:p.Leu149AlafsTer?
XM_005261069.3:c.480_481insG XP_005261126.1:p.Leu161AlafsTer?
XM_011529766.1:c.480_481insG XP_011528068.1:p.Leu161AlafsTer?
XM_011529767.1:c.441_442insG XP_011528069.1:p.Leu148AlafsTer?
XM_011529768.1:c.441_442insG XP_011528070.1:p.Leu148AlafsTer?
XM_011529770.1:c.480_481insG XP_011528072.1:p.Leu161AlafsTer?
XR_937576.1:n.659_660insG
XM_005261069.4:c.480_481insG XP_005261126.1:p.Leu161AlafsTer?
XM_011529766.2:c.480_481insG XP_011528068.1:p.Leu161AlafsTer?
XM_011529767.2:c.441_442insG XP_011528069.1:p.Leu148AlafsTer?
XM_011529768.2:c.441_442insG XP_011528070.1:p.Leu148AlafsTer?
XM_011529770.2:c.480_481insG XP_011528072.1:p.Leu161AlafsTer?
XM_017028487.1:c.327_328insG XP_016883976.1:p.Leu110AlafsTer?
XR_937576.2:n.706_707insG
NM_001001890.3:c.399_400insG NP_001001890.1:p.Leu134AlafsTer?
NM_001122607.2:c.399_400insG NP_001116079.1:p.Leu134AlafsTer?
NM_001754.5:c.480_481insG MANE Select NP_001745.2:p.Leu161AlafsTer?