Canonical Allele Identifier: CA2617607714

Gene: OLR1

Linked Data

• gnomAD v4: 12-10159714-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159714A>G , CM000674.2:g.10159714A>G	GRCh38
NC_000012.11:g.10312313A>G , CM000674.1:g.10312313A>G	GRCh37
NC_000012.10:g.10203580A>G	NCBI36
NG_016743.1:g.17478T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000309539.8:c.*166T>C MANE Select	ENSP00000309124.3:n.*166T>C
ENST00000309539.7:c.*166T>C	ENSP00000309124.3:n.*166T>C
ENST00000432556.6:c.*302T>C	ENSP00000405116.2:n.*302T>C
ENST00000536989.1:n.523T>C
ENST00000543993.5:c.*302T>C	ENSP00000445085.1:n.*302T>C
ENST00000544577.5:c.*166T>C	ENSP00000444457.1:n.*166T>C
ENST00000545927.5:c.*302T>C	ENSP00000439251.1:n.*302T>C
NM_001172632.1:c.*302T>C	NP_001166103.1:n.*302T>C
NM_001172633.1:c.*302T>C	NP_001166104.1:n.*302T>C
NM_002543.3:c.*166T>C	NP_002534.1:n.*166T>C
XM_011520682.1:c.*166T>C	XP_011518984.1:n.*166T>C
XM_011520683.1:c.*318T>C	XP_011518985.1:n.*318T>C
NM_002543.4:c.*166T>C MANE Select	NP_002534.1:n.*166T>C
NM_001172632.2:c.*302T>C	NP_001166103.1:n.*302T>C
NM_001172633.2:c.*302T>C	NP_001166104.1:n.*302T>C