Canonical Allele Identifier: CA2387297148

Gene: RUNX1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34886926C= , CM000683.2:g.34886926C=	GRCh38
NC_000021.8:g.36259223C= , CM000683.1:g.36259223C=	GRCh37
NC_000021.7:g.35181093C=	NCBI36
NG_011402.2:g.1102786G= , LRG_482:g.1102786G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675419.1:c.268G= MANE Select	ENSP00000501943.1:p.Val90=
ENST00000300305.7:c.268G=	ENSP00000300305.3:p.Val90=
ENST00000344691.8:c.187G=	ENSP00000340690.4:p.Val63=
ENST00000358356.9:c.187G=	ENSP00000351123.5:p.Val63=
ENST00000399237.6:c.232G=	ENSP00000382182.2:p.Val78=
ENST00000399240.5:c.187G=	ENSP00000382184.1:p.Val63=
ENST00000437180.5:c.268G=	ENSP00000409227.1:p.Val90=
ENST00000455571.5:c.229G=	ENSP00000388189.1:p.Val77=
ENST00000482318.5:c.59-6213G=	ENSP00000477067.1:n.59-6213G=
NM_001001890.2:c.187G=	NP_001001890.1:p.Val63=
NM_001122607.1:c.187G=	NP_001116079.1:p.Val63=
NM_001754.4:c.268G= , LRG_482t1:c.268G=	NP_001745.2:p.Val90=
XM_005261068.3:c.232G=	XP_005261125.1:p.Val78=
XM_005261069.3:c.268G=	XP_005261126.1:p.Val90=
XM_011529766.1:c.268G=	XP_011528068.1:p.Val90=
XM_011529767.1:c.229G=	XP_011528069.1:p.Val77=
XM_011529768.1:c.229G=	XP_011528070.1:p.Val77=
XM_011529770.1:c.268G=	XP_011528072.1:p.Val90=
XR_937576.1:n.447G=
XM_005261069.4:c.268G=	XP_005261126.1:p.Val90=
XM_011529766.2:c.268G=	XP_011528068.1:p.Val90=
XM_011529767.2:c.229G=	XP_011528069.1:p.Val77=
XM_011529768.2:c.229G=	XP_011528070.1:p.Val77=
XM_011529770.2:c.268G=	XP_011528072.1:p.Val90=
XM_017028487.1:c.115G=	XP_016883976.1:p.Val39=
XR_937576.2:n.494G=
NM_001001890.3:c.187G=	NP_001001890.1:p.Val63=
NM_001122607.2:c.187G=	NP_001116079.1:p.Val63=
NM_001754.5:c.268G= MANE Select	NP_001745.2:p.Val90=