Human (GRCh38.p14)
Description

apolipoprotein C2 [Source:HGNC Symbol;Acc:HGNC:609]

Location

Chromosome 19: 44,946,035-44,949,565 forward strand.

GRCh38:CM000681.2

About this gene

This gene has 5 transcripts (splice variants), 118 orthologues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000252490.7APOC2-201660101aaENSP00000252490.5
 
Protein coding
CCDS12650A0A024R0T9 P02655 NM_000483.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000585786.1APOC2-20288072aaENSP00000465001.1
 
Protein coding
Q6P163 -GENCODE basicTSL:2
ENST00000590360.2APOC2-203744101aaENSP00000466775.1
 
Protein coding
CCDS12650A0A024R0T9 P02655 -GENCODE basicAPPRIS P1TSL:3
ENST00000591597.5APOC2-20444787aaENSP00000476835.1
 
Protein coding
V9GYJ8 -GENCODE basicTSL:5
ENST00000592257.5APOC2-20544447aaENSP00000477261.1
 
Protein coding
V9GZ01 -GENCODE basicTSL:3