Canonical Allele Identifier: CA380469648

Gene: OR5L1

Linked Data

• MyVariant Identifiers: chr11:g.55579171A>T (hg19) ; chr11:g.55811695A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.55811695A>T , CM000673.2:g.55811695A>T	GRCh38
NC_000011.9:g.55579171A>T , CM000673.1:g.55579171A>T	GRCh37
NC_000011.8:g.55335747A>T	NCBI36
NG_052620.1:g.5329A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625203.2:c.229A>T MANE Select	ENSP00000485319.1:p.Ile77Phe
ENST00000333973.3:c.229A>T	ENSP00000335529.2:p.Ile77Phe
ENST00000623450.1:c.229A>T	ENSP00000485509.1:p.Ile77Phe
ENST00000625203.1:c.229A>T	ENSP00000485319.1:p.Ile77Phe
NM_001004738.1:c.229A>T	NP_001004738.1:p.Ile77Phe
NM_001004738.2:c.229A>T MANE Select	NP_001004738.1:p.Ile77Phe