Canonical Allele Identifier: CA2015815384
Gene: OLR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10159690G= , CM000674.2:g.10159690G= GRCh38
NC_000012.11:g.10312289G= , CM000674.1:g.10312289G= GRCh37
NC_000012.10:g.10203556G= NCBI36
NG_016743.1:g.17502C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309539.8:c.*190C= MANE Select ENSP00000309124.3:n.*190C=
ENST00000309539.7:c.*190C= ENSP00000309124.3:n.*190C=
ENST00000432556.6:c.*326C= ENSP00000405116.2:n.*326C=
ENST00000536989.1:n.547C=
ENST00000543993.5:c.*326C= ENSP00000445085.1:n.*326C=
ENST00000544577.5:c.*190C= ENSP00000444457.1:n.*190C=
ENST00000545927.5:c.*326C= ENSP00000439251.1:n.*326C=
NM_001172632.1:c.*326C= NP_001166103.1:n.*326C=
NM_001172633.1:c.*326C= NP_001166104.1:n.*326C=
NM_002543.3:c.*190C= NP_002534.1:n.*190C=
XM_011520682.1:c.*190C= XP_011518984.1:n.*190C=
XM_011520683.1:c.*342C= XP_011518985.1:n.*342C=
NM_002543.4:c.*190C= MANE Select NP_002534.1:n.*190C=
NM_001172632.2:c.*326C= NP_001166103.1:n.*326C=
NM_001172633.2:c.*326C= NP_001166104.1:n.*326C=