Advanced notice of Ensembl Tools maintenance
Please note that due to planned maintenance, Ensembl Tools will be unavailable from Tuesday, September 9, at 08:30 AM BST until Wednesday, September 10, at 08:30 AM BST.
Jobs submitted during the maintenance window will be queued and processed once maintenance is complete. We apologise for the inconvenience.

Human (GRCh38.p14)
Description

chromogranin A [Source:HGNC Symbol;Acc:HGNC:1929]

Gene Synonyms

PHE5, PHES

Location

Scaffold HSCHR14_7_CTG1: 37,642-49,855 forward strand.

GRCh38:KI270847.1

View this gene on the primary assembly.

About this gene

This gene has 6 transcripts (splice variants) and 1 gene allele.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000613166.3CHGA-2142063457aaENSP00000478198.1
 
Protein coding
P10645 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000630996.1CHGA-2181474306aaENSP00000486710.1
 
Protein coding
G5E968 -GENCODE BasicTSL:1
ENST00000627311.2CHGA-21589638aaENSP00000486340.1
 
Nonsense mediated decay
G3V2Q7 -TSL:5
ENST00000627696.1CHGA-216889No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000631274.1CHGA-219912No protein-
 
Retained intron
--TSL:2
ENST00000629687.1CHGA-217638No protein-
 
Retained intron
--TSL:3