Human (GRCh37.p13)
Description

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

Location

Chromosome 1: 212,738,676-212,794,119 forward strand.

GRCh37:CM000663.1

About this gene

This gene has 9 transcripts (splice variants) and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000341491.4ATF3-0012033181aaENSP00000344352.4
 
Protein coding
CCDS1506P18847 Q5VTZ4 NM_001674.3Ensembl CanonicalGENCODE Basic
ENST00000366987.2ATF3-2011896181aaENSP00000355954.2
 
Protein coding
CCDS1506P18847 Q5VTZ4 NM_001030287.3GENCODE Basic
ENST00000366983.1ATF3-004858135aaENSP00000355950.1
 
Protein coding
CCDS41464P18847 Q8NG55 -GENCODE Basic
ENST00000366981.4ATF3-002680175aaENSP00000355948.4
 
Protein coding
Q5VTZ4 -CDS 3' incomplete
ENST00000366985.1ATF3-007516124aaENSP00000355952.1
 
Protein coding
CCDS58059P18847 NM_001206484.2GENCODE Basic
ENST00000336937.4ATF3-006482106aaENSP00000336908.4
 
Protein coding
CCDS55688P18847 Q8NG55 NM_001206486.2GENCODE Basic
ENST00000464547.1ATF3-003767135aaENSP00000432208.1
 
Nonsense mediated decay
CCDS41464P18847 Q8NG55 --
ENST00000492118.1ATF3-0082117No protein-
 
Processed transcript
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ENST00000465155.1ATF3-0051626No protein-
 
Processed transcript
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