Human (GRCh38.p14)
Description

solute carrier family 27 member 5 [Source:HGNC Symbol;Acc:HGNC:10999]

Gene Synonyms

ACSB, ACSVL6, FACVL3, FATP5, FLJ22987, VLACSR, VLCS-H2, VLCSH2

Location

Chromosome 19: 58,479,512-58,512,413 reverse strand.

GRCh38:CM000681.2

About this gene

This gene has 8 transcripts (splice variants), 225 orthologues, 12 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000263093.7SLC27A5-2012292690aaENSP00000263093.2
 
Protein coding
CCDS12983Q9Y2P5-1 NM_012254.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000601355.1SLC27A5-2071987606aaENSP00000470368.1
 
Protein coding
CCDS82415Q9Y2P5-2 -GENCODE basicTSL:2
ENST00000594786.1SLC27A5-20464395aaENSP00000471065.1
 
Protein coding
M0R075 -GENCODE basicTSL:2
ENST00000595851.5SLC27A5-205200395aaENSP00000469512.1
 
Nonsense mediated decay
M0R075 -TSL:2
ENST00000599700.1SLC27A5-206474No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000593745.1SLC27A5-2025032No protein-
 
Retained intron
--TSL:NA
ENST00000601997.1SLC27A5-208575No protein-
 
Retained intron
--TSL:2
ENST00000594683.1SLC27A5-203564No protein-
 
Retained intron
--TSL:2