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Human (GRCh38.p14)
Description

phospholipase D family member 4 [Source:HGNC Symbol;Acc:HGNC:23792]

Gene Synonyms

C14ORF175

About this transcript

This transcript has 11 exons, is annotated with 18 domains and features, is associated with 4201 variant alleles and maps to 349 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000392593.9PLD4-2011905506aaENSP00000376372.5
 
Protein coding
CCDS9995Q96BZ4 NM_138790.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P2TSL:1
ENST00000649344.1PLD4-2072195455aaENSP00000497627.1
 
Protein coding
A0A3B3IT68 -GENCODE Basic
ENST00000862747.1PLD4-2092028506aaENSP00000532806.1
 
Protein coding
CCDS9995--GENCODE BasicAPPRIS P2
ENST00000540372.5PLD4-2042007513aaENSP00000438677.1
 
Protein coding
CCDS76725F5H2B5 -GENCODE BasicAPPRIS ALT2TSL:2
ENST00000862746.1PLD4-2081994506aaENSP00000532805.1
 
Protein coding
CCDS9995--GENCODE BasicAPPRIS P2
ENST00000557573.1PLD4-206883257aaENSP00000451278.1
 
Protein coding
G3V3J8 -TSL:3CDS 3' incomplete
ENST00000553861.1PLD4-20566775aaENSP00000451636.1
 
Protein coding
G3V472 -GENCODE PrimaryGENCODE BasicTSL:2
ENST00000472901.1PLD4-203691No protein-
 
Retained intron
--TSL:2
ENST00000472702.1PLD4-202628No protein-
 
Retained intron
--TSL:4
Statistics

Exons: 11, Coding exons: 10, Transcript length: 1,905 bps, Translation length: 506 residues

MANE

This MANE Select transcript contains ENSP00000376372 and matches to NM_138790.5 and NP_620145.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96BZ4

CCDS

This transcript is a member of the Human CCDS set: CCDS9995

Transcript Support Level (TSL)

TSL:1

Version

ENST00000392593.9

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.