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Human (GRCh38.p14)
Description

solute carrier family 27 member 6 [Source:HGNC Symbol;Acc:HGNC:11000]

Gene Synonyms

ACSVL2, FACVL2, FATP6, VLCS-H1

About this transcript

This transcript has 11 exons, is annotated with 16 domains and features, is associated with 31386 variant alleles and maps to 417 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000262462.9SLC27A6-2012863619aaENSP00000262462.4
 
Protein coding
CCDS4145Q9Y2P4 NM_001017372.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000395266.5SLC27A6-2022616619aaENSP00000378684.1
 
Protein coding
CCDS4145Q9Y2P4 -GENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000506176.1SLC27A6-2032294619aaENSP00000421024.1
 
Protein coding
CCDS4145Q9Y2P4 -GENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000508645.5SLC27A6-204811162aaENSP00000421759.1
 
Protein coding
D6RAJ2 -TSL:5CDS 3' incomplete
Statistics

Exons: 11, Coding exons: 10, Transcript length: 2,616 bps, Translation length: 619 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9Y2P4

CCDS

This transcript is a member of the Human CCDS set: CCDS4145

Transcript Support Level (TSL)

TSL:1

Version

ENST00000395266.5

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Annotation Attributes

alternative 5' UTR [Definitions]

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

GENCODE primary gene

This transcript is a member of the Gencode Primary gene set.