Canonical Allele Identifier: CA2617607711

Gene: OLR1

Linked Data

• gnomAD v4: 12-10159713-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159713C>A , CM000674.2:g.10159713C>A	GRCh38
NC_000012.11:g.10312312C>A , CM000674.1:g.10312312C>A	GRCh37
NC_000012.10:g.10203579C>A	NCBI36
NG_016743.1:g.17479G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000309539.8:c.*167G>T MANE Select	ENSP00000309124.3:n.*167G>T
ENST00000309539.7:c.*167G>T	ENSP00000309124.3:n.*167G>T
ENST00000432556.6:c.*303G>T	ENSP00000405116.2:n.*303G>T
ENST00000536989.1:n.524G>T
ENST00000543993.5:c.*303G>T	ENSP00000445085.1:n.*303G>T
ENST00000544577.5:c.*167G>T	ENSP00000444457.1:n.*167G>T
ENST00000545927.5:c.*303G>T	ENSP00000439251.1:n.*303G>T
NM_001172632.1:c.*303G>T	NP_001166103.1:n.*303G>T
NM_001172633.1:c.*303G>T	NP_001166104.1:n.*303G>T
NM_002543.3:c.*167G>T	NP_002534.1:n.*167G>T
XM_011520682.1:c.*167G>T	XP_011518984.1:n.*167G>T
XM_011520683.1:c.*319G>T	XP_011518985.1:n.*319G>T
NM_002543.4:c.*167G>T MANE Select	NP_002534.1:n.*167G>T
NM_001172632.2:c.*303G>T	NP_001166103.1:n.*303G>T
NM_001172633.2:c.*303G>T	NP_001166104.1:n.*303G>T