Human (GRCh38.p14)
Description

activating transcription factor 3 [Source:HGNC Symbol;Acc:HGNC:785]

Location

Chromosome 1: 212,565,334-212,620,777 forward strand.

GRCh38:CM000663.2

About this gene

This gene has 10 transcripts (splice variants), 214 orthologues and 8 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000341491.9ATF3-2021940181aaENSP00000344352.4
 
Protein coding
CCDS1506P18847-1 NM_001674.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000366987.6ATF3-2061917181aaENSP00000355954.2
 
Protein coding
CCDS1506P18847-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000366983.5ATF3-204858135aaENSP00000355950.1
 
Protein coding
CCDS41464P18847-3 -GENCODE basicTSL:1
ENST00000366981.8ATF3-203680175aaENSP00000355948.4
 
Protein coding
Q5VTZ4 -TSL:1CDS 3' incomplete
ENST00000613104.1ATF3-210581124aaENSP00000480606.1
 
Protein coding
CCDS58059P18847-5 -GENCODE basicTSL:1
ENST00000366985.5ATF3-205516153aaENSP00000355952.2
 
Protein coding
A0A0A0MRJ2 -TSL:5CDS 5' incomplete
ENST00000336937.8ATF3-201482106aaENSP00000336908.4
 
Protein coding
CCDS55688P18847-4 -GENCODE basicTSL:1
ENST00000464547.5ATF3-207767135aaENSP00000432208.1
 
Nonsense mediated decay
CCDS41464P18847-3 -TSL:1
ENST00000492118.2ATF3-2092103No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000465155.5ATF3-2081626No protein-
 
Retained intron
--TSL:2