Canonical Allele Identifier: CA645607324
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM24739

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880564_34880572dup , CM000683.2:g.34880564_34880572dup GRCh38
NC_000021.8:g.36252861_36252869dup , CM000683.1:g.36252861_36252869dup GRCh37
NC_000021.7:g.35174731_35174739dup NCBI36
NG_011402.2:g.1109142_1109150dup , LRG_482:g.1109142_1109150dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.495_503dup MANE Select ENSP00000501943.1:p.Gly168_Arg169insArgSerGly
ENST00000300305.7:c.495_503dup ENSP00000300305.3:p.Gly168_Arg169insArgSerGly
ENST00000344691.8:c.414_422dup ENSP00000340690.4:p.Gly141_Arg142insArgSerGly
ENST00000358356.9:c.414_422dup ENSP00000351123.5:p.Gly141_Arg142insArgSerGly
ENST00000399237.6:c.459_467dup ENSP00000382182.2:p.Gly156_Arg157insArgSerGly
ENST00000399240.5:c.414_422dup ENSP00000382184.1:p.Gly141_Arg142insArgSerGly
ENST00000437180.5:c.495_503dup ENSP00000409227.1:p.Gly168_Arg169insArgSerGly
ENST00000482318.5:c.*85_*93dup ENSP00000477067.1:n.*85_*93dup
NM_001001890.2:c.414_422dup NP_001001890.1:p.Gly141_Arg142insArgSerGly
NM_001122607.1:c.414_422dup NP_001116079.1:p.Gly141_Arg142insArgSerGly
NM_001754.4:c.495_503dup , LRG_482t1:c.495_503dup NP_001745.2:p.Gly168_Arg169insArgSerGly
XM_005261068.3:c.459_467dup XP_005261125.1:p.Gly156_Arg157insArgSerGly
XM_005261069.3:c.495_503dup XP_005261126.1:p.Gly168_Arg169insArgSerGly
XM_011529766.1:c.495_503dup XP_011528068.1:p.Gly168_Arg169insArgSerGly
XM_011529767.1:c.456_464dup XP_011528069.1:p.Gly155_Arg156insArgSerGly
XM_011529768.1:c.456_464dup XP_011528070.1:p.Gly155_Arg156insArgSerGly
XM_011529770.1:c.495_503dup XP_011528072.1:p.Gly168_Arg169insArgSerGly
XR_937576.1:n.674_682dup
XM_005261069.4:c.495_503dup XP_005261126.1:p.Gly168_Arg169insArgSerGly
XM_011529766.2:c.495_503dup XP_011528068.1:p.Gly168_Arg169insArgSerGly
XM_011529767.2:c.456_464dup XP_011528069.1:p.Gly155_Arg156insArgSerGly
XM_011529768.2:c.456_464dup XP_011528070.1:p.Gly155_Arg156insArgSerGly
XM_011529770.2:c.495_503dup XP_011528072.1:p.Gly168_Arg169insArgSerGly
XM_017028487.1:c.342_350dup XP_016883976.1:p.Gly117_Arg118insArgSerGly
XR_937576.2:n.721_729dup
NM_001001890.3:c.414_422dup NP_001001890.1:p.Gly141_Arg142insArgSerGly
NM_001122607.2:c.414_422dup NP_001116079.1:p.Gly141_Arg142insArgSerGly
NM_001754.5:c.495_503dup MANE Select NP_001745.2:p.Gly168_Arg169insArgSerGly