Canonical Allele Identifier: CA645607321
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM5944770
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880560_34880561insCCACTTC , CM000683.2:g.34880560_34880561insCCACTTC GRCh38
NC_000021.8:g.36252857_36252858insCCACTTC , CM000683.1:g.36252857_36252858insCCACTTC GRCh37
NC_000021.7:g.35174727_35174728insCCACTTC NCBI36
NG_011402.2:g.1109151_1109152insGAAGTGG , LRG_482:g.1109151_1109152insGAAGTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.504_505insGAAGTGG MANE Select ENSP00000501943.1:p.Arg169GlufsTer?
ENST00000300305.7:c.504_505insGAAGTGG ENSP00000300305.3:p.Arg169GlufsTer?
ENST00000344691.8:c.423_424insGAAGTGG ENSP00000340690.4:p.Arg142GlufsTer?
ENST00000358356.9:c.423_424insGAAGTGG ENSP00000351123.5:p.Arg142GlufsTer?
ENST00000399237.6:c.468_469insGAAGTGG ENSP00000382182.2:p.Arg157GlufsTer?
ENST00000399240.5:c.423_424insGAAGTGG ENSP00000382184.1:p.Arg142GlufsTer?
ENST00000437180.5:c.504_505insGAAGTGG ENSP00000409227.1:p.Arg169GlufsTer?
ENST00000482318.5:c.*94_*95insGAAGTGG ENSP00000477067.1:n.*94_*95insGAAGTGG
NM_001001890.2:c.423_424insGAAGTGG NP_001001890.1:p.Arg142GlufsTer?
NM_001122607.1:c.423_424insGAAGTGG NP_001116079.1:p.Arg142GlufsTer?
NM_001754.4:c.504_505insGAAGTGG , LRG_482t1:c.504_505insGAAGTGG NP_001745.2:p.Arg169GlufsTer?
XM_005261068.3:c.468_469insGAAGTGG XP_005261125.1:p.Arg157GlufsTer?
XM_005261069.3:c.504_505insGAAGTGG XP_005261126.1:p.Arg169GlufsTer?
XM_011529766.1:c.504_505insGAAGTGG XP_011528068.1:p.Arg169GlufsTer?
XM_011529767.1:c.465_466insGAAGTGG XP_011528069.1:p.Arg156GlufsTer?
XM_011529768.1:c.465_466insGAAGTGG XP_011528070.1:p.Arg156GlufsTer?
XM_011529770.1:c.504_505insGAAGTGG XP_011528072.1:p.Arg169GlufsTer?
XR_937576.1:n.683_684insGAAGTGG
XM_005261069.4:c.504_505insGAAGTGG XP_005261126.1:p.Arg169GlufsTer?
XM_011529766.2:c.504_505insGAAGTGG XP_011528068.1:p.Arg169GlufsTer?
XM_011529767.2:c.465_466insGAAGTGG XP_011528069.1:p.Arg156GlufsTer?
XM_011529768.2:c.465_466insGAAGTGG XP_011528070.1:p.Arg156GlufsTer?
XM_011529770.2:c.504_505insGAAGTGG XP_011528072.1:p.Arg169GlufsTer?
XM_017028487.1:c.351_352insGAAGTGG XP_016883976.1:p.Arg118GlufsTer?
XR_937576.2:n.730_731insGAAGTGG
NM_001001890.3:c.423_424insGAAGTGG NP_001001890.1:p.Arg142GlufsTer?
NM_001122607.2:c.423_424insGAAGTGG NP_001116079.1:p.Arg142GlufsTer?
NM_001754.5:c.504_505insGAAGTGG MANE Select NP_001745.2:p.Arg169GlufsTer?
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