Human (GRCh38.p14)
Description

BPI fold containing family B member 4 [Source:HGNC Symbol;Acc:HGNC:16179]

Gene Synonyms

C20ORF186, DJ726C3.5, LPLUNC4

Location
About this transcript

This transcript has 18 exons, is annotated with 14 domains and features, is associated with 14660 variant alleles and maps to 556 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000375483.4BPIFB4-2012343614aaENSP00000364632.3
 
Protein coding
CCDS13213P59827-1 NM_182519.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000674031.1BPIFB4-2042525736aaENSP00000501266.1
 
Protein coding
A0A669KBJ0 -GENCODE basic
ENST00000445356.1BPIFB4-20255444aaENSP00000388423.1
 
Nonsense mediated decay
F8WEG9 -TSL:2
ENST00000494121.1BPIFB4-203585No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 18, Coding exons: 16, Transcript length: 2,343 bps, Translation length: 614 residues

MANE

This MANE Select transcript contains ENSP00000364632 and matches to NM_182519.3 and NP_872325.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: P59827

CCDS

This transcript is a member of the Human CCDS set: CCDS13213

Transcript Support Level (TSL)

TSL:5

Version

ENST00000375483.4

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.