Canonical Allele Identifier: CA2015815385
Gene: OLR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10159691T= , CM000674.2:g.10159691T= GRCh38
NC_000012.11:g.10312290T= , CM000674.1:g.10312290T= GRCh37
NC_000012.10:g.10203557T= NCBI36
NG_016743.1:g.17501A=

Transcript Alleles

HGVS Amino-acid change
ENST00000309539.8:c.*189A= MANE Select ENSP00000309124.3:n.*189A=
ENST00000309539.7:c.*189A= ENSP00000309124.3:n.*189A=
ENST00000432556.6:c.*325A= ENSP00000405116.2:n.*325A=
ENST00000536989.1:n.546A=
ENST00000543993.5:c.*325A= ENSP00000445085.1:n.*325A=
ENST00000544577.5:c.*189A= ENSP00000444457.1:n.*189A=
ENST00000545927.5:c.*325A= ENSP00000439251.1:n.*325A=
NM_001172632.1:c.*325A= NP_001166103.1:n.*325A=
NM_001172633.1:c.*325A= NP_001166104.1:n.*325A=
NM_002543.3:c.*189A= NP_002534.1:n.*189A=
XM_011520682.1:c.*189A= XP_011518984.1:n.*189A=
XM_011520683.1:c.*341A= XP_011518985.1:n.*341A=
NM_002543.4:c.*189A= MANE Select NP_002534.1:n.*189A=
NM_001172632.2:c.*325A= NP_001166103.1:n.*325A=
NM_001172633.2:c.*325A= NP_001166104.1:n.*325A=