Canonical Allele Identifier: CA645607347
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880575_34880576insCT , CM000683.2:g.34880575_34880576insCT GRCh38
NC_000021.8:g.36252872_36252873insCT , CM000683.1:g.36252872_36252873insCT GRCh37
NC_000021.7:g.35174742_35174743insCT NCBI36
NG_011402.2:g.1109136_1109137insAG , LRG_482:g.1109136_1109137insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.489_490insAG MANE Select ENSP00000501943.1:p.Val164ArgfsTer13
ENST00000300305.7:c.489_490insAG ENSP00000300305.3:p.Val164ArgfsTer13
ENST00000344691.8:c.408_409insAG ENSP00000340690.4:p.Val137ArgfsTer13
ENST00000358356.9:c.408_409insAG ENSP00000351123.5:p.Val137ArgfsTer13
ENST00000399237.6:c.453_454insAG ENSP00000382182.2:p.Val152ArgfsTer13
ENST00000399240.5:c.408_409insAG ENSP00000382184.1:p.Val137ArgfsTer13
ENST00000437180.5:c.489_490insAG ENSP00000409227.1:p.Val164ArgfsTer13
ENST00000482318.5:c.*79_*80insAG ENSP00000477067.1:n.*79_*80insAG
NM_001001890.2:c.408_409insAG NP_001001890.1:p.Val137ArgfsTer13
NM_001122607.1:c.408_409insAG NP_001116079.1:p.Val137ArgfsTer13
NM_001754.4:c.489_490insAG , LRG_482t1:c.489_490insAG NP_001745.2:p.Val164ArgfsTer13
XM_005261068.3:c.453_454insAG XP_005261125.1:p.Val152ArgfsTer13
XM_005261069.3:c.489_490insAG XP_005261126.1:p.Val164ArgfsTer13
XM_011529766.1:c.489_490insAG XP_011528068.1:p.Val164ArgfsTer13
XM_011529767.1:c.450_451insAG XP_011528069.1:p.Val151ArgfsTer13
XM_011529768.1:c.450_451insAG XP_011528070.1:p.Val151ArgfsTer13
XM_011529770.1:c.489_490insAG XP_011528072.1:p.Val164ArgfsTer13
XR_937576.1:n.668_669insAG
XM_005261069.4:c.489_490insAG XP_005261126.1:p.Val164ArgfsTer13
XM_011529766.2:c.489_490insAG XP_011528068.1:p.Val164ArgfsTer13
XM_011529767.2:c.450_451insAG XP_011528069.1:p.Val151ArgfsTer13
XM_011529768.2:c.450_451insAG XP_011528070.1:p.Val151ArgfsTer13
XM_011529770.2:c.489_490insAG XP_011528072.1:p.Val164ArgfsTer13
XM_017028487.1:c.336_337insAG XP_016883976.1:p.Val113ArgfsTer13
XR_937576.2:n.715_716insAG
NM_001001890.3:c.408_409insAG NP_001001890.1:p.Val137ArgfsTer13
NM_001122607.2:c.408_409insAG NP_001116079.1:p.Val137ArgfsTer13
NM_001754.5:c.489_490insAG MANE Select NP_001745.2:p.Val164ArgfsTer13