Canonical Allele Identifier: CA2617607539

Gene: OLR1

Linked Data

• gnomAD v4: 12-10159599-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159599C>T , CM000674.2:g.10159599C>T	GRCh38
NC_000012.11:g.10312198C>T , CM000674.1:g.10312198C>T	GRCh37
NC_000012.10:g.10203465C>T	NCBI36
NG_016743.1:g.17593G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309539.8:c.*281G>A MANE Select	ENSP00000309124.3:n.*281G>A
ENST00000309539.7:c.*281G>A	ENSP00000309124.3:n.*281G>A
ENST00000543993.5:c.*417G>A	ENSP00000445085.1:n.*417G>A
ENST00000544577.5:c.*281G>A	ENSP00000444457.1:n.*281G>A
NM_001172632.1:c.*417G>A	NP_001166103.1:n.*417G>A
NM_001172633.1:c.*417G>A	NP_001166104.1:n.*417G>A
NM_002543.3:c.*281G>A	NP_002534.1:n.*281G>A
XM_011520682.1:c.*281G>A	XP_011518984.1:n.*281G>A
XM_011520683.1:c.*433G>A	XP_011518985.1:n.*433G>A
NM_002543.4:c.*281G>A MANE Select	NP_002534.1:n.*281G>A
NM_001172632.2:c.*417G>A	NP_001166103.1:n.*417G>A
NM_001172633.2:c.*417G>A	NP_001166104.1:n.*417G>A