Canonical Allele Identifier: CA2617607559

Gene: OLR1

Linked Data

• gnomAD v4: 12-10159624-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159624T>G , CM000674.2:g.10159624T>G	GRCh38
NC_000012.11:g.10312223T>G , CM000674.1:g.10312223T>G	GRCh37
NC_000012.10:g.10203490T>G	NCBI36
NG_016743.1:g.17568A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309539.8:c.*256A>C MANE Select	ENSP00000309124.3:n.*256A>C
ENST00000309539.7:c.*256A>C	ENSP00000309124.3:n.*256A>C
ENST00000543993.5:c.*392A>C	ENSP00000445085.1:n.*392A>C
ENST00000544577.5:c.*256A>C	ENSP00000444457.1:n.*256A>C
ENST00000545927.5:c.*392A>C	ENSP00000439251.1:n.*392A>C
NM_001172632.1:c.*392A>C	NP_001166103.1:n.*392A>C
NM_001172633.1:c.*392A>C	NP_001166104.1:n.*392A>C
NM_002543.3:c.*256A>C	NP_002534.1:n.*256A>C
XM_011520682.1:c.*256A>C	XP_011518984.1:n.*256A>C
XM_011520683.1:c.*408A>C	XP_011518985.1:n.*408A>C
NM_002543.4:c.*256A>C MANE Select	NP_002534.1:n.*256A>C
NM_001172632.2:c.*392A>C	NP_001166103.1:n.*392A>C
NM_001172633.2:c.*392A>C	NP_001166104.1:n.*392A>C