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Human (GRCh38.p14)
Description

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

Gene Synonyms

PHE5, PHES

Location
About this transcript

This transcript has 8 exons, is annotated with 33 domains and features, is associated with 5507 variant alleles and maps to 428 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000216492.10CHGA-2011985457aaENSP00000216492.5
 
Protein coding
CCDS9906P10645 NM_001275.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000334654.4CHGA-2021474306aaENSP00000334023.4
 
Protein coding
CCDS76718G5E968 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000556076.5CHGA-20489638aaENSP00000450801.1
 
Nonsense mediated decay
G3V2Q7 -TSL:5
ENST00000553866.1CHGA-203889No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000556876.1CHGA-206912No protein-
 
Retained intron
--TSL:2
ENST00000556098.1CHGA-205638No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 8, Coding exons: 8, Transcript length: 1,985 bps, Translation length: 457 residues

MANE

This MANE Select transcript contains ENSP00000216492 and matches to NM_001275.4 and NP_001266.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P10645

CCDS

This transcript is a member of the Human CCDS set: CCDS9906

Transcript Support Level (TSL)

TSL:1

Version

ENST00000216492.10

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.

GENCODE primary gene

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