Canonical Allele Identifier: CA474412755
Gene: OR5L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.55578984C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811508C>T , CM000673.2:g.55811508C>T GRCh38
NC_000011.9:g.55578984C>T , CM000673.1:g.55578984C>T GRCh37
NC_000011.8:g.55335560C>T NCBI36
NG_052620.1:g.5142C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.42C>T MANE Select ENSP00000485319.1:p.Leu14=
ENST00000333973.3:c.42C>T ENSP00000335529.2:p.Leu14=
ENST00000623450.1:c.42C>T ENSP00000485509.1:p.Leu14=
ENST00000625203.1:c.42C>T ENSP00000485319.1:p.Leu14=
NM_001004738.1:c.42C>T NP_001004738.1:p.Leu14=
NM_001004738.2:c.42C>T MANE Select NP_001004738.1:p.Leu14=