Canonical Allele Identifier: CA944669786

Gene: OLR1

Linked Data

• dbSNP Id: rs935182876
• gnomAD v3: 12-10159720-G-T
• gnomAD v4: 12-10159720-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159720G>T , CM000674.2:g.10159720G>T	GRCh38
NC_000012.11:g.10312319G>T , CM000674.1:g.10312319G>T	GRCh37
NC_000012.10:g.10203586G>T	NCBI36
NG_016743.1:g.17472C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000309539.8:c.*160C>A MANE Select	ENSP00000309124.3:n.*160C>A
ENST00000309539.7:c.*160C>A	ENSP00000309124.3:n.*160C>A
ENST00000432556.6:c.*296C>A	ENSP00000405116.2:n.*296C>A
ENST00000536989.1:n.517C>A
ENST00000543993.5:c.*296C>A	ENSP00000445085.1:n.*296C>A
ENST00000544577.5:c.*160C>A	ENSP00000444457.1:n.*160C>A
ENST00000545927.5:c.*296C>A	ENSP00000439251.1:n.*296C>A
NM_001172632.1:c.*296C>A	NP_001166103.1:n.*296C>A
NM_001172633.1:c.*296C>A	NP_001166104.1:n.*296C>A
NM_002543.3:c.*160C>A	NP_002534.1:n.*160C>A
XM_011520682.1:c.*160C>A	XP_011518984.1:n.*160C>A
XM_011520683.1:c.*312C>A	XP_011518985.1:n.*312C>A
NM_002543.4:c.*160C>A MANE Select	NP_002534.1:n.*160C>A
NM_001172632.2:c.*296C>A	NP_001166103.1:n.*296C>A
NM_001172633.2:c.*296C>A	NP_001166104.1:n.*296C>A