Canonical Allele Identifier: CA380774082

Gene: OR5A1

Linked Data

• MyVariant Identifiers: chr11:g.59211105G>T (hg19) ; chr11:g.59443632G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.59443632G>T , CM000673.2:g.59443632G>T	GRCh38
NC_000011.9:g.59211105G>T , CM000673.1:g.59211105G>T	GRCh37
NC_000011.8:g.58967681G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641045.1:c.464G>T MANE Select	ENSP00000493195.1:p.Gly155Val
ENST00000302030.2:c.464G>T	ENSP00000303096.2:p.Gly155Val
NM_001004728.1:c.464G>T	NP_001004728.1:p.Gly155Val
XM_011544810.1:c.464G>T	XP_011543112.1:p.Gly155Val
NM_001004728.2:c.464G>T MANE Select	NP_001004728.1:p.Gly155Val