Canonical Allele Identifier: CA2387297053

Gene: RUNX1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34886746A= , CM000683.2:g.34886746A=	GRCh38
NC_000021.8:g.36259043A= , CM000683.1:g.36259043A=	GRCh37
NC_000021.7:g.35180913A=	NCBI36
NG_011402.2:g.1102966T= , LRG_482:g.1102966T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675419.1:c.351+97T= MANE Select	ENSP00000501943.1:n.351+97T=
ENST00000300305.7:c.351+97T=	ENSP00000300305.3:n.351+97T=
ENST00000344691.8:c.270+97T=	ENSP00000340690.4:n.270+97T=
ENST00000358356.9:c.270+97T=	ENSP00000351123.5:n.270+97T=
ENST00000399237.6:c.315+97T=	ENSP00000382182.2:n.315+97T=
ENST00000399240.5:c.270+97T=	ENSP00000382184.1:n.270+97T=
ENST00000437180.5:c.351+97T=	ENSP00000409227.1:n.351+97T=
ENST00000455571.5:c.312+97T=	ENSP00000388189.1:n.312+97T=
ENST00000482318.5:c.59-6033T=	ENSP00000477067.1:n.59-6033T=
NM_001001890.2:c.270+97T=	NP_001001890.1:n.270+97T=
NM_001122607.1:c.270+97T=	NP_001116079.1:n.270+97T=
NM_001754.4:c.351+97T= , LRG_482t1:c.351+97T=	NP_001745.2:n.351+97T=
XM_005261068.3:c.315+97T=	XP_005261125.1:n.315+97T=
XM_005261069.3:c.351+97T=	XP_005261126.1:n.351+97T=
XM_011529766.1:c.351+97T=	XP_011528068.1:n.351+97T=
XM_011529767.1:c.312+97T=	XP_011528069.1:n.312+97T=
XM_011529768.1:c.312+97T=	XP_011528070.1:n.312+97T=
XM_011529770.1:c.351+97T=	XP_011528072.1:n.351+97T=
XR_937576.1:n.530+97T=
XM_005261069.4:c.351+97T=	XP_005261126.1:n.351+97T=
XM_011529766.2:c.351+97T=	XP_011528068.1:n.351+97T=
XM_011529767.2:c.312+97T=	XP_011528069.1:n.312+97T=
XM_011529768.2:c.312+97T=	XP_011528070.1:n.312+97T=
XM_011529770.2:c.351+97T=	XP_011528072.1:n.351+97T=
XM_017028487.1:c.198+97T=	XP_016883976.1:n.198+97T=
XR_937576.2:n.577+97T=
NM_001001890.3:c.270+97T=	NP_001001890.1:n.270+97T=
NM_001122607.2:c.270+97T=	NP_001116079.1:n.270+97T=
NM_001754.5:c.351+97T= MANE Select	NP_001745.2:n.351+97T=