Description

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

Location
INSDC coordinates

chromosome:GRCh38:CM000664.2:21001429:21044073:1

Transcripts

This gene has 3 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
APOB-001ENST00000233242141214563 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS1703P04114 Q13828 Q9UE51
Q9UE52 Q9UE53 S5FVK9
NM_000384
NP_000375
TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS PIAPPRIS principal isoform
Glossary entry for APPRIS
APPRIS website
APOB-201ENST00000616098139914344 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-Q13828 Q9UE51 Q9UE52
Q9UE53 S5FVK9
-TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
APOB-002ENST000003992563128828 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-A8MUN2 -TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

Gene-based displays