Human (GRCh38.p14)
Description

apolipoprotein A2 [Source:HGNC Symbol;Acc:HGNC:601]

Location

Chromosome 1: 161,222,292-161,223,631 reverse strand.

GRCh38:CM000663.2

About this gene

This gene has 10 transcripts (splice variants), 86 orthologues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000367990.7APOA2-201474100aaENSP00000356969.3
 
Protein coding
CCDS1226P02652 NM_001643.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000464492.5APOA2-204530133aaENSP00000476911.1
 
Protein coding
V9GYM3 -GENCODE basicTSL:3
ENST00000463273.5APOA2-20246995aaENSP00000476740.1
 
Protein coding
V9GYG9 -TSL:1CDS 3' incomplete
ENST00000468465.5APOA2-20542152aaENSP00000476662.1
 
Protein coding
V9GYE3 -GENCODE basicTSL:2
ENST00000470459.6APOA2-20741682aaENSP00000477031.1
 
Protein coding
V9GYS1 -GENCODE basicTSL:5
ENST00000463812.1APOA2-20340152aaENSP00000476890.1
 
Protein coding
V9GYE3 -GENCODE basicTSL:2
ENST00000469730.2APOA2-20626566aaENSP00000476605.1
 
Protein coding
V9GYC1 -TSL:5CDS 3' incomplete
ENST00000491350.1APOA2-21026327aaENSP00000477353.1
 
Protein coding
Q76EI7 -GENCODE basicTSL:1
ENST00000481511.5APOA2-20965572aaENSP00000477054.1
 
Nonsense mediated decay
V9GYT0 -TSL:5
ENST00000481413.1APOA2-208927No protein-
 
Retained intron
--TSL:2