Human (GRCh38.p14)
Description

apolipoprotein B [Source:HGNC Symbol;Acc:HGNC:603]

Location
About this transcript

This transcript has 17 exons, is annotated with 17 domains and features, is associated with 9594 variant alleles and maps to 345 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000233242.5APOB-201141214563aaENSP00000233242.1
 
Protein coding
CCDS1703P04114 NM_000384.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000399256.4APOB-2023128828aaENSP00000382200.4
 
Protein coding
A8MUN2 -GENCODE basicTSL:1
ENST00000673739.2APOB-2035489179aaENSP00000501110.2
 
Nonsense mediated decay
A0A669KB70 --
ENST00000673882.2APOB-2043840179aaENSP00000501253.2
 
Nonsense mediated decay
A0A669KB70 --
Statistics

Exons: 17, Coding exons: 17, Transcript length: 3,128 bps, Translation length: 828 residues

Transcript Support Level (TSL)

TSL:1

Version

ENST00000399256.4

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.