Canonical Allele Identifier: CA5992737

Gene: OR5L1

Linked Data

• dbSNP Id: rs779202859
• ExAC: 11:55579386 C / A
• gnomAD v2: 11-55579386-C-A
• gnomAD v4: 11-55811910-C-A
• MyVariant Identifiers: chr11:g.55579386C>A (hg19) ; chr11:g.55811910C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.55811910C>A , CM000673.2:g.55811910C>A	GRCh38
NC_000011.9:g.55579386C>A , CM000673.1:g.55579386C>A	GRCh37
NC_000011.8:g.55335962C>A	NCBI36
NG_052620.1:g.5544C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625203.2:c.444C>A MANE Select	ENSP00000485319.1:p.Cys148Ter
ENST00000333973.3:c.444C>A	ENSP00000335529.2:p.Cys148Ter
ENST00000623450.1:c.444C>A	ENSP00000485509.1:p.Cys148Ter
ENST00000625203.1:c.444C>A	ENSP00000485319.1:p.Cys148Ter
NM_001004738.1:c.444C>A	NP_001004738.1:p.Cys148Ter
NM_001004738.2:c.444C>A MANE Select	NP_001004738.1:p.Cys148Ter