Canonical Allele Identifier: CA645607450

Gene: RUNX1

Linked Data

• COSMIC: COSM36062

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34886949_34886950insAGCAA , CM000683.2:g.34886949_34886950insAGCAA	GRCh38
NC_000021.8:g.36259246_36259247insAGCAA , CM000683.1:g.36259246_36259247insAGCAA	GRCh37
NC_000021.7:g.35181116_35181117insAGCAA	NCBI36
NG_011402.2:g.1102763_1102764insTGCTT , LRG_482:g.1102763_1102764insTGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675419.1:c.245_246insTGCTT MANE Select	ENSP00000501943.1:p.Asp84TrpfsTer?
ENST00000300305.7:c.245_246insTGCTT	ENSP00000300305.3:p.Asp84TrpfsTer?
ENST00000344691.8:c.164_165insTGCTT	ENSP00000340690.4:p.Asp57TrpfsTer?
ENST00000358356.9:c.164_165insTGCTT	ENSP00000351123.5:p.Asp57TrpfsTer?
ENST00000399237.6:c.209_210insTGCTT	ENSP00000382182.2:p.Asp72TrpfsTer?
ENST00000399240.5:c.164_165insTGCTT	ENSP00000382184.1:p.Asp57TrpfsTer?
ENST00000437180.5:c.245_246insTGCTT	ENSP00000409227.1:p.Asp84TrpfsTer?
ENST00000455571.5:c.206_207insTGCTT	ENSP00000388189.1:p.Asp71TrpfsTer?
ENST00000482318.5:c.59-6236_59-6235insTGCTT	ENSP00000477067.1:n.59-6236_59-6235insTGCTT
NM_001001890.2:c.164_165insTGCTT	NP_001001890.1:p.Asp57TrpfsTer?
NM_001122607.1:c.164_165insTGCTT	NP_001116079.1:p.Asp57TrpfsTer?
NM_001754.4:c.245_246insTGCTT , LRG_482t1:c.245_246insTGCTT	NP_001745.2:p.Asp84TrpfsTer?
XM_005261068.3:c.209_210insTGCTT	XP_005261125.1:p.Asp72TrpfsTer?
XM_005261069.3:c.245_246insTGCTT	XP_005261126.1:p.Asp84TrpfsTer?
XM_011529766.1:c.245_246insTGCTT	XP_011528068.1:p.Asp84TrpfsTer?
XM_011529767.1:c.206_207insTGCTT	XP_011528069.1:p.Asp71TrpfsTer?
XM_011529768.1:c.206_207insTGCTT	XP_011528070.1:p.Asp71TrpfsTer?
XM_011529770.1:c.245_246insTGCTT	XP_011528072.1:p.Asp84TrpfsTer?
XR_937576.1:n.424_425insTGCTT
XM_005261069.4:c.245_246insTGCTT	XP_005261126.1:p.Asp84TrpfsTer?
XM_011529766.2:c.245_246insTGCTT	XP_011528068.1:p.Asp84TrpfsTer?
XM_011529767.2:c.206_207insTGCTT	XP_011528069.1:p.Asp71TrpfsTer?
XM_011529768.2:c.206_207insTGCTT	XP_011528070.1:p.Asp71TrpfsTer?
XM_011529770.2:c.245_246insTGCTT	XP_011528072.1:p.Asp84TrpfsTer?
XM_017028487.1:c.92_93insTGCTT	XP_016883976.1:p.Asp33TrpfsTer?
XR_937576.2:n.471_472insTGCTT
NM_001001890.3:c.164_165insTGCTT	NP_001001890.1:p.Asp57TrpfsTer?
NM_001122607.2:c.164_165insTGCTT	NP_001116079.1:p.Asp57TrpfsTer?
NM_001754.5:c.245_246insTGCTT MANE Select	NP_001745.2:p.Asp84TrpfsTer?