Canonical Allele Identifier: CA2794523712
Gene: OLR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10159607G>T , CM000674.2:g.10159607G>T GRCh38
NC_000012.11:g.10312206G>T , CM000674.1:g.10312206G>T GRCh37
NC_000012.10:g.10203473G>T NCBI36
NG_016743.1:g.17585C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000309539.8:c.*273C>A MANE Select ENSP00000309124.3:n.*273C>A
ENST00000309539.7:c.*273C>A ENSP00000309124.3:n.*273C>A
ENST00000543993.5:c.*409C>A ENSP00000445085.1:n.*409C>A
ENST00000544577.5:c.*273C>A ENSP00000444457.1:n.*273C>A
NM_001172632.1:c.*409C>A NP_001166103.1:n.*409C>A
NM_001172633.1:c.*409C>A NP_001166104.1:n.*409C>A
NM_002543.3:c.*273C>A NP_002534.1:n.*273C>A
XM_011520682.1:c.*273C>A XP_011518984.1:n.*273C>A
XM_011520683.1:c.*425C>A XP_011518985.1:n.*425C>A
NM_002543.4:c.*273C>A MANE Select NP_002534.1:n.*273C>A
NM_001172632.2:c.*409C>A NP_001166103.1:n.*409C>A
NM_001172633.2:c.*409C>A NP_001166104.1:n.*409C>A