Canonical Allele Identifier: CA478445267
Gene: OLR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10160849C>T , CM000674.2:g.10160849C>T GRCh38
NC_000012.11:g.10313448C>T , CM000674.1:g.10313448C>T GRCh37
NC_000012.10:g.10204715C>T NCBI36
NG_016743.1:g.16343G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309539.8:c.501G>A MANE Select ENSP00000309124.3:p.Lys167=
ENST00000309539.7:c.501G>A ENSP00000309124.3:p.Lys167=
ENST00000339968.6:c.189G>A ENSP00000340572.6:p.Lys63=
ENST00000432556.6:c.425-387G>A ENSP00000405116.2:n.425-387G>A
ENST00000538745.5:c.189G>A ENSP00000438925.2:p.Lys63=
ENST00000539518.5:c.342G>A ENSP00000442389.1:p.Lys114=
ENST00000543993.5:c.113-387G>A ENSP00000445085.1:n.113-387G>A
ENST00000544577.5:c.425-896G>A ENSP00000444457.1:n.425-896G>A
ENST00000545927.5:c.501G>A ENSP00000439251.1:p.Lys167=
NM_001172632.1:c.425-387G>A NP_001166103.1:n.425-387G>A
NM_001172633.1:c.501G>A NP_001166104.1:p.Lys167=
NM_002543.3:c.501G>A NP_002534.1:p.Lys167=
XM_011520682.1:c.501G>A XP_011518984.1:p.Lys167=
XM_011520683.1:c.501G>A XP_011518985.1:p.Lys167=
NM_002543.4:c.501G>A MANE Select NP_002534.1:p.Lys167=
NM_001172632.2:c.425-387G>A NP_001166103.1:n.425-387G>A
NM_001172633.2:c.501G>A NP_001166104.1:p.Lys167=