Canonical Allele Identifier: CA2387257524

Gene: RUNX1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34799407G= , CM000683.2:g.34799407G=	GRCh38
NC_000021.8:g.36171704G= , CM000683.1:g.36171704G=	GRCh37
NC_000021.7:g.35093574G=	NCBI36
NG_011402.2:g.1190305C= , LRG_482:g.1190305C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001754.5:c.861C= MANE Select	NP_001745.2:p.Tyr287=
ENST00000675419.1:c.861C= MANE Select	ENSP00000501943.1:p.Tyr287=
NM_001001890.2:c.780C=	NP_001001890.1:p.Tyr260=
NM_001001890.3:c.780C=	NP_001001890.1:p.Tyr260=
NM_001754.4:c.861C= , LRG_482t1:c.861C=	NP_001745.2:p.Tyr287=
ENST00000300305.7:c.861C=	ENSP00000300305.3:p.Tyr287=
ENST00000344691.8:c.780C=	ENSP00000340690.4:p.Tyr260=
ENST00000399240.5:c.588C=	ENSP00000382184.1:p.Tyr196=
ENST00000437180.5:c.861C=	ENSP00000409227.1:p.Tyr287=
ENST00000482318.5:c.*451C=	ENSP00000477067.1:n.*451C=
XM_005261068.3:c.825C=	XP_005261125.1:p.Tyr275=
XM_005261069.3:c.669C=	XP_005261126.1:p.Tyr223=
XM_005261069.4:c.669C=	XP_005261126.1:p.Tyr223=
XM_011529766.1:c.861C=	XP_011528068.1:p.Tyr287=
XM_011529766.2:c.861C=	XP_011528068.1:p.Tyr287=
XM_011529767.1:c.822C=	XP_011528069.1:p.Tyr274=
XM_011529767.2:c.822C=	XP_011528069.1:p.Tyr274=
XM_011529768.1:c.630C=	XP_011528070.1:p.Tyr210=
XM_011529768.2:c.630C=	XP_011528070.1:p.Tyr210=
XM_017028487.1:c.708C=	XP_016883976.1:p.Tyr236=
XR_937576.1:n.1040C=
XR_937576.2:n.1087C=