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Human (GRCh38.p14)
Description

phospholipid transfer protein [Source:HGNC Symbol;Acc:HGNC:9093]

Gene Synonyms

BPIFE

Location
About this transcript

This transcript has 15 exons, is annotated with 23 domains and features, is associated with 6447 variant alleles and maps to 542 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000372431.8PLTP-2031889493aaENSP00000361508.3
 
Protein coding
CCDS13386P55058-1 NM_006227.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000477313.5PLTP-2052255493aaENSP00000417138.1
 
Protein coding
CCDS13386P55058-1 -GENCODE BasicAPPRIS P1TSL:1
ENST00000354050.8PLTP-2011731441aaENSP00000335290.4
 
Protein coding
CCDS13387P55058-2 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000372420.5PLTP-2021530405aaENSP00000361497.1
 
Protein coding
CCDS56196P55058-4 -GENCODE BasicTSL:2
ENST00000420868.2PLTP-2041420398aaENSP00000411671.2
 
Protein coding
CCDS56197P55058-3 -GENCODE BasicTSL:2
Statistics

Exons: 15, Coding exons: 14, Transcript length: 1,731 bps, Translation length: 441 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P55058

CCDS

This transcript is a member of the Human CCDS set: CCDS13387

Transcript Support Level (TSL)

TSL:1

Version

ENST00000354050.8

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.

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.