Canonical Allele Identifier: CA645607423
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM25138

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886860_34886862dup , CM000683.2:g.34886860_34886862dup GRCh38
NC_000021.8:g.36259157_36259159dup , CM000683.1:g.36259157_36259159dup GRCh37
NC_000021.7:g.35181027_35181029dup NCBI36
NG_011402.2:g.1102850_1102852dup , LRG_482:g.1102850_1102852dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.332_334dup MANE Select ENSP00000501943.1:p.Thr111_Leu112insPro
ENST00000300305.7:c.332_334dup ENSP00000300305.3:p.Thr111_Leu112insPro
ENST00000344691.8:c.251_253dup ENSP00000340690.4:p.Thr84_Leu85insPro
ENST00000358356.9:c.251_253dup ENSP00000351123.5:p.Thr84_Leu85insPro
ENST00000399237.6:c.296_298dup ENSP00000382182.2:p.Thr99_Leu100insPro
ENST00000399240.5:c.251_253dup ENSP00000382184.1:p.Thr84_Leu85insPro
ENST00000437180.5:c.332_334dup ENSP00000409227.1:p.Thr111_Leu112insPro
ENST00000455571.5:c.293_295dup ENSP00000388189.1:p.Thr98_Leu99insPro
ENST00000482318.5:c.59-6149_59-6147dup ENSP00000477067.1:n.59-6149_59-6147dup
NM_001001890.2:c.251_253dup NP_001001890.1:p.Thr84_Leu85insPro
NM_001122607.1:c.251_253dup NP_001116079.1:p.Thr84_Leu85insPro
NM_001754.4:c.332_334dup , LRG_482t1:c.332_334dup NP_001745.2:p.Thr111_Leu112insPro
XM_005261068.3:c.296_298dup XP_005261125.1:p.Thr99_Leu100insPro
XM_005261069.3:c.332_334dup XP_005261126.1:p.Thr111_Leu112insPro
XM_011529766.1:c.332_334dup XP_011528068.1:p.Thr111_Leu112insPro
XM_011529767.1:c.293_295dup XP_011528069.1:p.Thr98_Leu99insPro
XM_011529768.1:c.293_295dup XP_011528070.1:p.Thr98_Leu99insPro
XM_011529770.1:c.332_334dup XP_011528072.1:p.Thr111_Leu112insPro
XR_937576.1:n.511_513dup
XM_005261069.4:c.332_334dup XP_005261126.1:p.Thr111_Leu112insPro
XM_011529766.2:c.332_334dup XP_011528068.1:p.Thr111_Leu112insPro
XM_011529767.2:c.293_295dup XP_011528069.1:p.Thr98_Leu99insPro
XM_011529768.2:c.293_295dup XP_011528070.1:p.Thr98_Leu99insPro
XM_011529770.2:c.332_334dup XP_011528072.1:p.Thr111_Leu112insPro
XM_017028487.1:c.179_181dup XP_016883976.1:p.Thr60_Leu61insPro
XR_937576.2:n.558_560dup
NM_001001890.3:c.251_253dup NP_001001890.1:p.Thr84_Leu85insPro
NM_001122607.2:c.251_253dup NP_001116079.1:p.Thr84_Leu85insPro
NM_001754.5:c.332_334dup MANE Select NP_001745.2:p.Thr111_Leu112insPro