Canonical Allele Identifier: CA380774136
Gene: OR5A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.59443640A>C , CM000673.2:g.59443640A>C GRCh38
NC_000011.9:g.59211113A>C , CM000673.1:g.59211113A>C GRCh37
NC_000011.8:g.58967689A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641045.1:c.472A>C MANE Select ENSP00000493195.1:p.Ser158Arg
ENST00000302030.2:c.472A>C ENSP00000303096.2:p.Ser158Arg
NM_001004728.1:c.472A>C NP_001004728.1:p.Ser158Arg
XM_011544810.1:c.472A>C XP_011543112.1:p.Ser158Arg
NM_001004728.2:c.472A>C MANE Select NP_001004728.1:p.Ser158Arg