Canonical Allele Identifier: CA474412711
Gene: OR5L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.55578957C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811481C>T , CM000673.2:g.55811481C>T GRCh38
NC_000011.9:g.55578957C>T , CM000673.1:g.55578957C>T GRCh37
NC_000011.8:g.55335533C>T NCBI36
NG_052620.1:g.5115C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.15C>T MANE Select ENSP00000485319.1:p.Asn5=
ENST00000333973.3:c.15C>T ENSP00000335529.2:p.Asn5=
ENST00000623450.1:c.15C>T ENSP00000485509.1:p.Asn5=
ENST00000625203.1:c.15C>T ENSP00000485319.1:p.Asn5=
NM_001004738.1:c.15C>T NP_001004738.1:p.Asn5=
NM_001004738.2:c.15C>T MANE Select NP_001004738.1:p.Asn5=