Canonical Allele Identifier: CA2838033013

Gene: RUNX1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34886959_34886961delinsAGCGTCC , CM000683.2:g.34886959_34886961delinsAGCGTCC	GRCh38
NC_000021.8:g.36259256_36259258delinsAGCGTCC , CM000683.1:g.36259256_36259258delinsAGCGTCC	GRCh37
NC_000021.7:g.35181126_35181128delinsAGCGTCC	NCBI36
NG_011402.2:g.1102751_1102753delinsGGACGCT , LRG_482:g.1102751_1102753delinsGGACGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675419.1:c.233_235delinsGGACGCT MANE Select	ENSP00000501943.1:p.Met78ArgfsTer?
ENST00000300305.7:c.233_235delinsGGACGCT	ENSP00000300305.3:p.Met78ArgfsTer?
ENST00000344691.8:c.152_154delinsGGACGCT	ENSP00000340690.4:p.Met51ArgfsTer?
ENST00000358356.9:c.152_154delinsGGACGCT	ENSP00000351123.5:p.Met51ArgfsTer?
ENST00000399237.6:c.197_199delinsGGACGCT	ENSP00000382182.2:p.Met66ArgfsTer?
ENST00000399240.5:c.152_154delinsGGACGCT	ENSP00000382184.1:p.Met51ArgfsTer?
ENST00000437180.5:c.233_235delinsGGACGCT	ENSP00000409227.1:p.Met78ArgfsTer?
ENST00000455571.5:c.194_196delinsGGACGCT	ENSP00000388189.1:p.Met65ArgfsTer?
ENST00000482318.5:c.59-6248_59-6246delinsGGACGCT	ENSP00000477067.1:n.59-6248_59-6246delinsGGACGCT
NM_001001890.2:c.152_154delinsGGACGCT	NP_001001890.1:p.Met51ArgfsTer?
NM_001122607.1:c.152_154delinsGGACGCT	NP_001116079.1:p.Met51ArgfsTer?
NM_001754.4:c.233_235delinsGGACGCT , LRG_482t1:c.233_235delinsGGACGCT	NP_001745.2:p.Met78ArgfsTer?
XM_005261068.3:c.197_199delinsGGACGCT	XP_005261125.1:p.Met66ArgfsTer?
XM_005261069.3:c.233_235delinsGGACGCT	XP_005261126.1:p.Met78ArgfsTer?
XM_011529766.1:c.233_235delinsGGACGCT	XP_011528068.1:p.Met78ArgfsTer?
XM_011529767.1:c.194_196delinsGGACGCT	XP_011528069.1:p.Met65ArgfsTer?
XM_011529768.1:c.194_196delinsGGACGCT	XP_011528070.1:p.Met65ArgfsTer?
XM_011529770.1:c.233_235delinsGGACGCT	XP_011528072.1:p.Met78ArgfsTer?
XR_937576.1:n.412_414delinsGGACGCT
XM_005261069.4:c.233_235delinsGGACGCT	XP_005261126.1:p.Met78ArgfsTer?
XM_011529766.2:c.233_235delinsGGACGCT	XP_011528068.1:p.Met78ArgfsTer?
XM_011529767.2:c.194_196delinsGGACGCT	XP_011528069.1:p.Met65ArgfsTer?
XM_011529768.2:c.194_196delinsGGACGCT	XP_011528070.1:p.Met65ArgfsTer?
XM_011529770.2:c.233_235delinsGGACGCT	XP_011528072.1:p.Met78ArgfsTer?
XM_017028487.1:c.80_82delinsGGACGCT	XP_016883976.1:p.Met27ArgfsTer?
XR_937576.2:n.459_461delinsGGACGCT
NM_001001890.3:c.152_154delinsGGACGCT	NP_001001890.1:p.Met51ArgfsTer?
NM_001122607.2:c.152_154delinsGGACGCT	NP_001116079.1:p.Met51ArgfsTer?
NM_001754.5:c.233_235delinsGGACGCT MANE Select	NP_001745.2:p.Met78ArgfsTer?