We need your help! Has Ensembl saved you time or effort? Please take 15 minutes to fill in a survey and help EMBL-EBI make the case for why open data resources are critical to life science research.
https://www.surveymonkey.com/r/QGFMBH8?channel=[webpage]

Human (GRCh38.p14)
Description

paraoxonase 1 [Source:HGNC Symbol;Acc:HGNC:9204]

Gene Synonyms

ESA, PON

Location
About this transcript

This transcript has 9 exons, is annotated with 22 domains and features, is associated with 11686 variant alleles and maps to 520 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000222381.8PON1-2012393355aaENSP00000222381.3
 
Protein coding
CCDS5638P27169 NM_000446.7MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000433729.1PON1-202105877aaENSP00000407359.1
 
Nonsense mediated decay
F8WF42 -TSL:3
ENST00000470502.1PON1-204578No protein-
 
Retained intron
--TSL:4
ENST00000462594.1PON1-203553No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 9, Coding exons: 9, Transcript length: 2,393 bps, Translation length: 355 residues

MANE

This MANE Select transcript contains ENSP00000222381 and matches to NM_000446.7 and NP_000437.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: P27169

CCDS

This transcript is a member of the Human CCDS set: CCDS5638

Transcript Support Level (TSL)

TSL:1

Version

ENST00000222381.8

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.