Canonical Allele Identifier: CA5992751
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs758248920
ExAC: 11:55579470 CT / C
gnomAD v2: 11-55579470-CT-C
MyVariant Identifiers: chr11:g.55579471del (hg19) chr11:g.55811995del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811999del , CM000673.2:g.55811999del GRCh38
NC_000011.9:g.55579475del , CM000673.1:g.55579475del GRCh37
NC_000011.8:g.55336051del NCBI36
NG_052620.1:g.5633del

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.533del MANE Select ENSP00000485319.1:p.Phe178SerfsTer8
ENST00000333973.3:c.533del ENSP00000335529.2:p.Phe178SerfsTer8
ENST00000623450.1:c.533del ENSP00000485509.1:p.Phe178SerfsTer8
ENST00000625203.1:c.533del ENSP00000485319.1:p.Phe178SerfsTer8
NM_001004738.1:c.533del NP_001004738.1:p.Phe178SerfsTer8
NM_001004738.2:c.533del MANE Select NP_001004738.1:p.Phe178SerfsTer8
Search 100 bp 5'
Search 100 bp 3'