Canonical Allele Identifier: CA2841244241

Gene: RUNX1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34886969_34886970insCGACCGCAGCATGGTGGAGGTGC , CM000683.2:g.34886969_34886970insCGACCGCAGCATGGTGGAGGTGC	GRCh38
NC_000021.8:g.36259266_36259267insCGACCGCAGCATGGTGGAGGTGC , CM000683.1:g.36259266_36259267insCGACCGCAGCATGGTGGAGGTGC	GRCh37
NC_000021.7:g.35181136_35181137insCGACCGCAGCATGGTGGAGGTGC	NCBI36
NG_011402.2:g.1102742_1102743insGCACCTCCACCATGCTGCGGTCG , LRG_482:g.1102742_1102743insGCACCTCCACCATGCTGCGGTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675419.1:c.224_225insGCACCTCCACCATGCTGCGGTCG MANE Select	ENSP00000501943.1:p.Asp75GlufsTer?
ENST00000300305.7:c.224_225insGCACCTCCACCATGCTGCGGTCG	ENSP00000300305.3:p.Asp75GlufsTer?
ENST00000344691.8:c.143_144insGCACCTCCACCATGCTGCGGTCG	ENSP00000340690.4:p.Asp48GlufsTer?
ENST00000358356.9:c.143_144insGCACCTCCACCATGCTGCGGTCG	ENSP00000351123.5:p.Asp48GlufsTer?
ENST00000399237.6:c.188_189insGCACCTCCACCATGCTGCGGTCG	ENSP00000382182.2:p.Asp63GlufsTer?
ENST00000399240.5:c.143_144insGCACCTCCACCATGCTGCGGTCG	ENSP00000382184.1:p.Asp48GlufsTer?
ENST00000437180.5:c.224_225insGCACCTCCACCATGCTGCGGTCG	ENSP00000409227.1:p.Asp75GlufsTer?
ENST00000455571.5:c.185_186insGCACCTCCACCATGCTGCGGTCG	ENSP00000388189.1:p.Asp62GlufsTer?
ENST00000482318.5:c.59-6257_59-6256insGCACCTCCACCATGCTGCGGTCG	ENSP00000477067.1:n.59-6257_59-6256insGCACCTCCACCATGCTGCGGTCG...
NM_001001890.2:c.143_144insGCACCTCCACCATGCTGCGGTCG	NP_001001890.1:p.Asp48GlufsTer?
NM_001122607.1:c.143_144insGCACCTCCACCATGCTGCGGTCG	NP_001116079.1:p.Asp48GlufsTer?
NM_001754.4:c.224_225insGCACCTCCACCATGCTGCGGTCG , LRG_482t1:c.224_225insGCACCTCCACCATGCTGCGGTCG	NP_001745.2:p.Asp75GlufsTer?
XM_005261068.3:c.188_189insGCACCTCCACCATGCTGCGGTCG	XP_005261125.1:p.Asp63GlufsTer?
XM_005261069.3:c.224_225insGCACCTCCACCATGCTGCGGTCG	XP_005261126.1:p.Asp75GlufsTer?
XM_011529766.1:c.224_225insGCACCTCCACCATGCTGCGGTCG	XP_011528068.1:p.Asp75GlufsTer?
XM_011529767.1:c.185_186insGCACCTCCACCATGCTGCGGTCG	XP_011528069.1:p.Asp62GlufsTer?
XM_011529768.1:c.185_186insGCACCTCCACCATGCTGCGGTCG	XP_011528070.1:p.Asp62GlufsTer?
XM_011529770.1:c.224_225insGCACCTCCACCATGCTGCGGTCG	XP_011528072.1:p.Asp75GlufsTer?
XR_937576.1:n.403_404insGCACCTCCACCATGCTGCGGTCG
XM_005261069.4:c.224_225insGCACCTCCACCATGCTGCGGTCG	XP_005261126.1:p.Asp75GlufsTer?
XM_011529766.2:c.224_225insGCACCTCCACCATGCTGCGGTCG	XP_011528068.1:p.Asp75GlufsTer?
XM_011529767.2:c.185_186insGCACCTCCACCATGCTGCGGTCG	XP_011528069.1:p.Asp62GlufsTer?
XM_011529768.2:c.185_186insGCACCTCCACCATGCTGCGGTCG	XP_011528070.1:p.Asp62GlufsTer?
XM_011529770.2:c.224_225insGCACCTCCACCATGCTGCGGTCG	XP_011528072.1:p.Asp75GlufsTer?
XM_017028487.1:c.71_72insGCACCTCCACCATGCTGCGGTCG	XP_016883976.1:p.Asp24GlufsTer?
XR_937576.2:n.450_451insGCACCTCCACCATGCTGCGGTCG
NM_001001890.3:c.143_144insGCACCTCCACCATGCTGCGGTCG	NP_001001890.1:p.Asp48GlufsTer?
NM_001122607.2:c.143_144insGCACCTCCACCATGCTGCGGTCG	NP_001116079.1:p.Asp48GlufsTer?
NM_001754.5:c.224_225insGCACCTCCACCATGCTGCGGTCG MANE Select	NP_001745.2:p.Asp75GlufsTer?