Canonical Allele Identifier: CA2015815360
Gene: OLR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10159634A= , CM000674.2:g.10159634A= GRCh38
NC_000012.11:g.10312233A= , CM000674.1:g.10312233A= GRCh37
NC_000012.10:g.10203500A= NCBI36
NG_016743.1:g.17558T=

Transcript Alleles

HGVS Amino-acid change
ENST00000309539.8:c.*246T= MANE Select ENSP00000309124.3:n.*246T=
ENST00000309539.7:c.*246T= ENSP00000309124.3:n.*246T=
ENST00000543993.5:c.*382T= ENSP00000445085.1:n.*382T=
ENST00000544577.5:c.*246T= ENSP00000444457.1:n.*246T=
ENST00000545927.5:c.*382T= ENSP00000439251.1:n.*382T=
NM_001172632.1:c.*382T= NP_001166103.1:n.*382T=
NM_001172633.1:c.*382T= NP_001166104.1:n.*382T=
NM_002543.3:c.*246T= NP_002534.1:n.*246T=
XM_011520682.1:c.*246T= XP_011518984.1:n.*246T=
XM_011520683.1:c.*398T= XP_011518985.1:n.*398T=
NM_002543.4:c.*246T= MANE Select NP_002534.1:n.*246T=
NM_001172632.2:c.*382T= NP_001166103.1:n.*382T=
NM_001172633.2:c.*382T= NP_001166104.1:n.*382T=