Canonical Allele Identifier: CA380468700

Gene: OR5L1

Linked Data

• gnomAD v4: 11-55811560-C-T
• MyVariant Identifiers: chr11:g.55579036C>T (hg19) ; chr11:g.55811560C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.55811560C>T , CM000673.2:g.55811560C>T	GRCh38
NC_000011.9:g.55579036C>T , CM000673.1:g.55579036C>T	GRCh37
NC_000011.8:g.55335612C>T	NCBI36
NG_052620.1:g.5194C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625203.2:c.94C>T MANE Select	ENSP00000485319.1:p.Leu32Phe
ENST00000333973.3:c.94C>T	ENSP00000335529.2:p.Leu32Phe
ENST00000623450.1:c.94C>T	ENSP00000485509.1:p.Leu32Phe
ENST00000625203.1:c.94C>T	ENSP00000485319.1:p.Leu32Phe
NM_001004738.1:c.94C>T	NP_001004738.1:p.Leu32Phe
NM_001004738.2:c.94C>T MANE Select	NP_001004738.1:p.Leu32Phe