Canonical Allele Identifier: CA2617607683

Gene: OLR1

Linked Data

• gnomAD v4: 12-10159700-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159700T>G , CM000674.2:g.10159700T>G	GRCh38
NC_000012.11:g.10312299T>G , CM000674.1:g.10312299T>G	GRCh37
NC_000012.10:g.10203566T>G	NCBI36
NG_016743.1:g.17492A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000309539.8:c.*180A>C MANE Select	ENSP00000309124.3:n.*180A>C
ENST00000309539.7:c.*180A>C	ENSP00000309124.3:n.*180A>C
ENST00000432556.6:c.*316A>C	ENSP00000405116.2:n.*316A>C
ENST00000536989.1:n.537A>C
ENST00000543993.5:c.*316A>C	ENSP00000445085.1:n.*316A>C
ENST00000544577.5:c.*180A>C	ENSP00000444457.1:n.*180A>C
ENST00000545927.5:c.*316A>C	ENSP00000439251.1:n.*316A>C
NM_001172632.1:c.*316A>C	NP_001166103.1:n.*316A>C
NM_001172633.1:c.*316A>C	NP_001166104.1:n.*316A>C
NM_002543.3:c.*180A>C	NP_002534.1:n.*180A>C
XM_011520682.1:c.*180A>C	XP_011518984.1:n.*180A>C
XM_011520683.1:c.*332A>C	XP_011518985.1:n.*332A>C
NM_002543.4:c.*180A>C MANE Select	NP_002534.1:n.*180A>C
NM_001172632.2:c.*316A>C	NP_001166103.1:n.*316A>C
NM_001172633.2:c.*316A>C	NP_001166104.1:n.*316A>C