Canonical Allele Identifier: CA2015815390

Gene: OLR1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159714A= , CM000674.2:g.10159714A=	GRCh38
NC_000012.11:g.10312313A= , CM000674.1:g.10312313A=	GRCh37
NC_000012.10:g.10203580A=	NCBI36
NG_016743.1:g.17478T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309539.8:c.*166T= MANE Select	ENSP00000309124.3:n.*166T=
ENST00000309539.7:c.*166T=	ENSP00000309124.3:n.*166T=
ENST00000432556.6:c.*302T=	ENSP00000405116.2:n.*302T=
ENST00000536989.1:n.523T=
ENST00000543993.5:c.*302T=	ENSP00000445085.1:n.*302T=
ENST00000544577.5:c.*166T=	ENSP00000444457.1:n.*166T=
ENST00000545927.5:c.*302T=	ENSP00000439251.1:n.*302T=
NM_001172632.1:c.*302T=	NP_001166103.1:n.*302T=
NM_001172633.1:c.*302T=	NP_001166104.1:n.*302T=
NM_002543.3:c.*166T=	NP_002534.1:n.*166T=
XM_011520682.1:c.*166T=	XP_011518984.1:n.*166T=
XM_011520683.1:c.*318T=	XP_011518985.1:n.*318T=
NM_002543.4:c.*166T= MANE Select	NP_002534.1:n.*166T=
NM_001172632.2:c.*302T=	NP_001166103.1:n.*302T=
NM_001172633.2:c.*302T=	NP_001166104.1:n.*302T=