Canonical Allele Identifier: CA512318786
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880698_34880699insG , CM000683.2:g.34880698_34880699insG GRCh38
NC_000021.8:g.36252995_36252996insG , CM000683.1:g.36252995_36252996insG GRCh37
NC_000021.7:g.35174865_35174866insG NCBI36
NG_011402.2:g.1109013_1109014insC , LRG_482:g.1109013_1109014insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.366_367insC MANE Select ENSP00000501943.1:p.Asp123ArgfsTer15
ENST00000300305.7:c.366_367insC ENSP00000300305.3:p.Asp123ArgfsTer15
ENST00000344691.8:c.285_286insC ENSP00000340690.4:p.Asp96ArgfsTer15
ENST00000358356.9:c.285_286insC ENSP00000351123.5:p.Asp96ArgfsTer15
ENST00000399237.6:c.330_331insC ENSP00000382182.2:p.Asp111ArgfsTer15
ENST00000399240.5:c.285_286insC ENSP00000382184.1:p.Asp96ArgfsTer15
ENST00000437180.5:c.366_367insC ENSP00000409227.1:p.Asp123ArgfsTer15
ENST00000455571.5:c.327_328insC ENSP00000388189.1:p.Asp110ArgfsTer15
ENST00000482318.5:c.73_74insC ENSP00000477067.1:p.Gly25AlafsTer11
NM_001001890.2:c.285_286insC NP_001001890.1:p.Asp96ArgfsTer15
NM_001122607.1:c.285_286insC NP_001116079.1:p.Asp96ArgfsTer15
NM_001754.4:c.366_367insC , LRG_482t1:c.366_367insC NP_001745.2:p.Asp123ArgfsTer15
XM_005261068.3:c.330_331insC XP_005261125.1:p.Asp111ArgfsTer15
XM_005261069.3:c.366_367insC XP_005261126.1:p.Asp123ArgfsTer15
XM_011529766.1:c.366_367insC XP_011528068.1:p.Asp123ArgfsTer15
XM_011529767.1:c.327_328insC XP_011528069.1:p.Asp110ArgfsTer15
XM_011529768.1:c.327_328insC XP_011528070.1:p.Asp110ArgfsTer15
XM_011529770.1:c.366_367insC XP_011528072.1:p.Asp123ArgfsTer15
XR_937576.1:n.545_546insC
XM_005261069.4:c.366_367insC XP_005261126.1:p.Asp123ArgfsTer15
XM_011529766.2:c.366_367insC XP_011528068.1:p.Asp123ArgfsTer15
XM_011529767.2:c.327_328insC XP_011528069.1:p.Asp110ArgfsTer15
XM_011529768.2:c.327_328insC XP_011528070.1:p.Asp110ArgfsTer15
XM_011529770.2:c.366_367insC XP_011528072.1:p.Asp123ArgfsTer15
XM_017028487.1:c.213_214insC XP_016883976.1:p.Asp72ArgfsTer15
XR_937576.2:n.592_593insC
NM_001001890.3:c.285_286insC NP_001001890.1:p.Asp96ArgfsTer15
NM_001122607.2:c.285_286insC NP_001116079.1:p.Asp96ArgfsTer15
NM_001754.5:c.366_367insC MANE Select NP_001745.2:p.Asp123ArgfsTer15