Canonical Allele Identifier: CA5992734

Gene: OR5L1

Linked Data

• dbSNP Id: rs190758912
• ExAC: 11:55579375 G / A
• gnomAD v2: 11-55579375-G-A
• gnomAD v3: 11-55811899-G-A
• gnomAD v4: 11-55811899-G-A
• COSMIC: COSM5070847
• MyVariant Identifiers: chr11:g.55579375G>A (hg19) ; chr11:g.55811899G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.55811899G>A , CM000673.2:g.55811899G>A	GRCh38
NC_000011.9:g.55579375G>A , CM000673.1:g.55579375G>A	GRCh37
NC_000011.8:g.55335951G>A	NCBI36
NG_052620.1:g.5533G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625203.2:c.433G>A MANE Select	ENSP00000485319.1:p.Ala145Thr
ENST00000333973.3:c.433G>A	ENSP00000335529.2:p.Ala145Thr
ENST00000623450.1:c.433G>A	ENSP00000485509.1:p.Ala145Thr
ENST00000625203.1:c.433G>A	ENSP00000485319.1:p.Ala145Thr
NM_001004738.1:c.433G>A	NP_001004738.1:p.Ala145Thr
NM_001004738.2:c.433G>A MANE Select	NP_001004738.1:p.Ala145Thr