Human (GRCh38.p14)
Description

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

Location
About this transcript

This transcript has 29 exons, is annotated with 32 domains and features, is associated with 24170 variant alleles and maps to 1106 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: 29, Coding exons: 29, Transcript length: 14,121 bps, Translation length: 4,563 residues

MANE

This MANE Select transcript contains ENSP00000233242 and matches to NM_000384.3 and NP_000375.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: P04114

CCDS

This transcript is a member of the Human CCDS set: CCDS1703

Transcript Support Level (TSL)

TSL:1

Version

ENST00000233242.5

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.

GENCODE basic gene

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