Canonical Allele Identifier: CA2015815739

Gene: OLR1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10160535G= , CM000674.2:g.10160535G=	GRCh38
NC_000012.11:g.10313134G= , CM000674.1:g.10313134G=	GRCh37
NC_000012.10:g.10204401G=	NCBI36
NG_016743.1:g.16657C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309539.8:c.565-73C= MANE Select	ENSP00000309124.3:n.565-73C=
ENST00000309539.7:c.565-73C=	ENSP00000309124.3:n.565-73C=
ENST00000339968.6:c.253-73C=	ENSP00000340572.6:n.253-73C=
ENST00000432556.6:c.425-73C=	ENSP00000405116.2:n.425-73C=
ENST00000536989.1:n.27C=
ENST00000538745.5:c.253-73C=	ENSP00000438925.2:n.253-73C=
ENST00000539518.5:c.406-73C=	ENSP00000442389.1:n.406-73C=
ENST00000543993.5:c.113-73C=	ENSP00000445085.1:n.113-73C=
ENST00000544577.5:c.425-582C=	ENSP00000444457.1:n.425-582C=
ENST00000545927.5:c.564+251C=	ENSP00000439251.1:n.564+251C=
NM_001172632.1:c.425-73C=	NP_001166103.1:n.425-73C=
NM_001172633.1:c.564+251C=	NP_001166104.1:n.564+251C=
NM_002543.3:c.565-73C=	NP_002534.1:n.565-73C=
XM_011520682.1:c.565-73C=	XP_011518984.1:n.565-73C=
XM_011520683.1:c.565-20C=	XP_011518985.1:n.565-20C=
NM_002543.4:c.565-73C= MANE Select	NP_002534.1:n.565-73C=
NM_001172632.2:c.425-73C=	NP_001166103.1:n.425-73C=
NM_001172633.2:c.564+251C=	NP_001166104.1:n.564+251C=