Canonical Allele Identifier: CA654124389

Gene: OLR1

Linked Data

• gnomAD v4: 12-10159630-G-A
• COSMIC: COSN8585174

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159630G>A , CM000674.2:g.10159630G>A	GRCh38
NC_000012.11:g.10312229G>A , CM000674.1:g.10312229G>A	GRCh37
NC_000012.10:g.10203496G>A	NCBI36
NG_016743.1:g.17562C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000309539.8:c.*250C>T MANE Select	ENSP00000309124.3:n.*250C>T
ENST00000309539.7:c.*250C>T	ENSP00000309124.3:n.*250C>T
ENST00000543993.5:c.*386C>T	ENSP00000445085.1:n.*386C>T
ENST00000544577.5:c.*250C>T	ENSP00000444457.1:n.*250C>T
ENST00000545927.5:c.*386C>T	ENSP00000439251.1:n.*386C>T
NM_001172632.1:c.*386C>T	NP_001166103.1:n.*386C>T
NM_001172633.1:c.*386C>T	NP_001166104.1:n.*386C>T
NM_002543.3:c.*250C>T	NP_002534.1:n.*250C>T
XM_011520682.1:c.*250C>T	XP_011518984.1:n.*250C>T
XM_011520683.1:c.*402C>T	XP_011518985.1:n.*402C>T
NM_002543.4:c.*250C>T MANE Select	NP_002534.1:n.*250C>T
NM_001172632.2:c.*386C>T	NP_001166103.1:n.*386C>T
NM_001172633.2:c.*386C>T	NP_001166104.1:n.*386C>T