Canonical Allele Identifier: CA645607434
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM26018

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886895dup , CM000683.2:g.34886895dup GRCh38
NC_000021.8:g.36259192dup , CM000683.1:g.36259192dup GRCh37
NC_000021.7:g.35181062dup NCBI36
NG_011402.2:g.1102818dup , LRG_482:g.1102818dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.300dup MANE Select ENSP00000501943.1:p.Val101ArgfsTer?
ENST00000300305.7:c.300dup ENSP00000300305.3:p.Val101ArgfsTer?
ENST00000344691.8:c.219dup ENSP00000340690.4:p.Val74ArgfsTer?
ENST00000358356.9:c.219dup ENSP00000351123.5:p.Val74ArgfsTer?
ENST00000399237.6:c.264dup ENSP00000382182.2:p.Val89ArgfsTer?
ENST00000399240.5:c.219dup ENSP00000382184.1:p.Val74ArgfsTer?
ENST00000437180.5:c.300dup ENSP00000409227.1:p.Val101ArgfsTer?
ENST00000455571.5:c.261dup ENSP00000388189.1:p.Val88ArgfsTer?
ENST00000482318.5:c.59-6181dup ENSP00000477067.1:n.59-6181dup
NM_001001890.2:c.219dup NP_001001890.1:p.Val74ArgfsTer?
NM_001122607.1:c.219dup NP_001116079.1:p.Val74ArgfsTer?
NM_001754.4:c.300dup , LRG_482t1:c.300dup NP_001745.2:p.Val101ArgfsTer?
XM_005261068.3:c.264dup XP_005261125.1:p.Val89ArgfsTer?
XM_005261069.3:c.300dup XP_005261126.1:p.Val101ArgfsTer?
XM_011529766.1:c.300dup XP_011528068.1:p.Val101ArgfsTer?
XM_011529767.1:c.261dup XP_011528069.1:p.Val88ArgfsTer?
XM_011529768.1:c.261dup XP_011528070.1:p.Val88ArgfsTer?
XM_011529770.1:c.300dup XP_011528072.1:p.Val101ArgfsTer?
XR_937576.1:n.479dup
XM_005261069.4:c.300dup XP_005261126.1:p.Val101ArgfsTer?
XM_011529766.2:c.300dup XP_011528068.1:p.Val101ArgfsTer?
XM_011529767.2:c.261dup XP_011528069.1:p.Val88ArgfsTer?
XM_011529768.2:c.261dup XP_011528070.1:p.Val88ArgfsTer?
XM_011529770.2:c.300dup XP_011528072.1:p.Val101ArgfsTer?
XM_017028487.1:c.147dup XP_016883976.1:p.Val50ArgfsTer?
XR_937576.2:n.526dup
NM_001001890.3:c.219dup NP_001001890.1:p.Val74ArgfsTer?
NM_001122607.2:c.219dup NP_001116079.1:p.Val74ArgfsTer?
NM_001754.5:c.300dup MANE Select NP_001745.2:p.Val101ArgfsTer?