Canonical Allele Identifier: CA2617607725

Gene: OLR1

Linked Data

• gnomAD v4: 12-10159718-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159718A>T , CM000674.2:g.10159718A>T	GRCh38
NC_000012.11:g.10312317A>T , CM000674.1:g.10312317A>T	GRCh37
NC_000012.10:g.10203584A>T	NCBI36
NG_016743.1:g.17474T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309539.8:c.*162T>A MANE Select	ENSP00000309124.3:n.*162T>A
ENST00000309539.7:c.*162T>A	ENSP00000309124.3:n.*162T>A
ENST00000432556.6:c.*298T>A	ENSP00000405116.2:n.*298T>A
ENST00000536989.1:n.519T>A
ENST00000543993.5:c.*298T>A	ENSP00000445085.1:n.*298T>A
ENST00000544577.5:c.*162T>A	ENSP00000444457.1:n.*162T>A
ENST00000545927.5:c.*298T>A	ENSP00000439251.1:n.*298T>A
NM_001172632.1:c.*298T>A	NP_001166103.1:n.*298T>A
NM_001172633.1:c.*298T>A	NP_001166104.1:n.*298T>A
NM_002543.3:c.*162T>A	NP_002534.1:n.*162T>A
XM_011520682.1:c.*162T>A	XP_011518984.1:n.*162T>A
XM_011520683.1:c.*314T>A	XP_011518985.1:n.*314T>A
NM_002543.4:c.*162T>A MANE Select	NP_002534.1:n.*162T>A
NM_001172632.2:c.*298T>A	NP_001166103.1:n.*298T>A
NM_001172633.2:c.*298T>A	NP_001166104.1:n.*298T>A