Canonical Allele Identifier: CA380472089
Gene: OR5L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.55579471T>A (hg19) chr11:g.55811995T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811995T>A , CM000673.2:g.55811995T>A GRCh38
NC_000011.9:g.55579471T>A , CM000673.1:g.55579471T>A GRCh37
NC_000011.8:g.55336047T>A NCBI36
NG_052620.1:g.5629T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.529T>A MANE Select ENSP00000485319.1:p.Phe177Ile
ENST00000333973.3:c.529T>A ENSP00000335529.2:p.Phe177Ile
ENST00000623450.1:c.529T>A ENSP00000485509.1:p.Phe177Ile
ENST00000625203.1:c.529T>A ENSP00000485319.1:p.Phe177Ile
NM_001004738.1:c.529T>A NP_001004738.1:p.Phe177Ile
NM_001004738.2:c.529T>A MANE Select NP_001004738.1:p.Phe177Ile
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