Canonical Allele Identifier: CA645607339
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880573_34880575dup , CM000683.2:g.34880573_34880575dup GRCh38
NC_000021.8:g.36252870_36252872dup , CM000683.1:g.36252870_36252872dup GRCh37
NC_000021.7:g.35174740_35174742dup NCBI36
NG_011402.2:g.1109138_1109140dup , LRG_482:g.1109138_1109140dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.491_493dup MANE Select ENSP00000501943.1:p.Val164_Gly165insVal
ENST00000300305.7:c.491_493dup ENSP00000300305.3:p.Val164_Gly165insVal
ENST00000344691.8:c.410_412dup ENSP00000340690.4:p.Val137_Gly138insVal
ENST00000358356.9:c.410_412dup ENSP00000351123.5:p.Val137_Gly138insVal
ENST00000399237.6:c.455_457dup ENSP00000382182.2:p.Val152_Gly153insVal
ENST00000399240.5:c.410_412dup ENSP00000382184.1:p.Val137_Gly138insVal
ENST00000437180.5:c.491_493dup ENSP00000409227.1:p.Val164_Gly165insVal
ENST00000482318.5:c.*81_*83dup ENSP00000477067.1:n.*81_*83dup
NM_001001890.2:c.410_412dup NP_001001890.1:p.Val137_Gly138insVal
NM_001122607.1:c.410_412dup NP_001116079.1:p.Val137_Gly138insVal
NM_001754.4:c.491_493dup , LRG_482t1:c.491_493dup NP_001745.2:p.Val164_Gly165insVal
XM_005261068.3:c.455_457dup XP_005261125.1:p.Val152_Gly153insVal
XM_005261069.3:c.491_493dup XP_005261126.1:p.Val164_Gly165insVal
XM_011529766.1:c.491_493dup XP_011528068.1:p.Val164_Gly165insVal
XM_011529767.1:c.452_454dup XP_011528069.1:p.Val151_Gly152insVal
XM_011529768.1:c.452_454dup XP_011528070.1:p.Val151_Gly152insVal
XM_011529770.1:c.491_493dup XP_011528072.1:p.Val164_Gly165insVal
XR_937576.1:n.670_672dup
XM_005261069.4:c.491_493dup XP_005261126.1:p.Val164_Gly165insVal
XM_011529766.2:c.491_493dup XP_011528068.1:p.Val164_Gly165insVal
XM_011529767.2:c.452_454dup XP_011528069.1:p.Val151_Gly152insVal
XM_011529768.2:c.452_454dup XP_011528070.1:p.Val151_Gly152insVal
XM_011529770.2:c.491_493dup XP_011528072.1:p.Val164_Gly165insVal
XM_017028487.1:c.338_340dup XP_016883976.1:p.Val113_Gly114insVal
XR_937576.2:n.717_719dup
NM_001001890.3:c.410_412dup NP_001001890.1:p.Val137_Gly138insVal
NM_001122607.2:c.410_412dup NP_001116079.1:p.Val137_Gly138insVal
NM_001754.5:c.491_493dup MANE Select NP_001745.2:p.Val164_Gly165insVal