Canonical Allele Identifier: CA2617607562

Gene: OLR1

Linked Data

• gnomAD v4: 12-10159626-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159626A>C , CM000674.2:g.10159626A>C	GRCh38
NC_000012.11:g.10312225A>C , CM000674.1:g.10312225A>C	GRCh37
NC_000012.10:g.10203492A>C	NCBI36
NG_016743.1:g.17566T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309539.8:c.*254T>G MANE Select	ENSP00000309124.3:n.*254T>G
ENST00000309539.7:c.*254T>G	ENSP00000309124.3:n.*254T>G
ENST00000543993.5:c.*390T>G	ENSP00000445085.1:n.*390T>G
ENST00000544577.5:c.*254T>G	ENSP00000444457.1:n.*254T>G
ENST00000545927.5:c.*390T>G	ENSP00000439251.1:n.*390T>G
NM_001172632.1:c.*390T>G	NP_001166103.1:n.*390T>G
NM_001172633.1:c.*390T>G	NP_001166104.1:n.*390T>G
NM_002543.3:c.*254T>G	NP_002534.1:n.*254T>G
XM_011520682.1:c.*254T>G	XP_011518984.1:n.*254T>G
XM_011520683.1:c.*406T>G	XP_011518985.1:n.*406T>G
NM_002543.4:c.*254T>G MANE Select	NP_002534.1:n.*254T>G
NM_001172632.2:c.*390T>G	NP_001166103.1:n.*390T>G
NM_001172633.2:c.*390T>G	NP_001166104.1:n.*390T>G