Canonical Allele Identifier: CA645607430

Gene: RUNX1

Linked Data

• COSMIC: COSM5879787 ; COSM5879788

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34886884dup , CM000683.2:g.34886884dup	GRCh38
NC_000021.8:g.36259181dup , CM000683.1:g.36259181dup	GRCh37
NC_000021.7:g.35181051dup	NCBI36
NG_011402.2:g.1102828dup , LRG_482:g.1102828dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675419.1:c.310dup MANE Select	ENSP00000501943.1:p.Thr104AsnfsTer?
ENST00000300305.7:c.310dup	ENSP00000300305.3:p.Thr104AsnfsTer?
ENST00000344691.8:c.229dup	ENSP00000340690.4:p.Thr77AsnfsTer?
ENST00000358356.9:c.229dup	ENSP00000351123.5:p.Thr77AsnfsTer?
ENST00000399237.6:c.274dup	ENSP00000382182.2:p.Thr92AsnfsTer?
ENST00000399240.5:c.229dup	ENSP00000382184.1:p.Thr77AsnfsTer?
ENST00000437180.5:c.310dup	ENSP00000409227.1:p.Thr104AsnfsTer?
ENST00000455571.5:c.271dup	ENSP00000388189.1:p.Thr91AsnfsTer?
ENST00000482318.5:c.59-6171dup	ENSP00000477067.1:n.59-6171dup
NM_001001890.2:c.229dup	NP_001001890.1:p.Thr77AsnfsTer?
NM_001122607.1:c.229dup	NP_001116079.1:p.Thr77AsnfsTer?
NM_001754.4:c.310dup , LRG_482t1:c.310dup	NP_001745.2:p.Thr104AsnfsTer?
XM_005261068.3:c.274dup	XP_005261125.1:p.Thr92AsnfsTer?
XM_005261069.3:c.310dup	XP_005261126.1:p.Thr104AsnfsTer?
XM_011529766.1:c.310dup	XP_011528068.1:p.Thr104AsnfsTer?
XM_011529767.1:c.271dup	XP_011528069.1:p.Thr91AsnfsTer?
XM_011529768.1:c.271dup	XP_011528070.1:p.Thr91AsnfsTer?
XM_011529770.1:c.310dup	XP_011528072.1:p.Thr104AsnfsTer?
XR_937576.1:n.489dup
XM_005261069.4:c.310dup	XP_005261126.1:p.Thr104AsnfsTer?
XM_011529766.2:c.310dup	XP_011528068.1:p.Thr104AsnfsTer?
XM_011529767.2:c.271dup	XP_011528069.1:p.Thr91AsnfsTer?
XM_011529768.2:c.271dup	XP_011528070.1:p.Thr91AsnfsTer?
XM_011529770.2:c.310dup	XP_011528072.1:p.Thr104AsnfsTer?
XM_017028487.1:c.157dup	XP_016883976.1:p.Thr53AsnfsTer?
XR_937576.2:n.536dup
NM_001001890.3:c.229dup	NP_001001890.1:p.Thr77AsnfsTer?
NM_001122607.2:c.229dup	NP_001116079.1:p.Thr77AsnfsTer?
NM_001754.5:c.310dup MANE Select	NP_001745.2:p.Thr104AsnfsTer?