Human (GRCh38.p14)
Description

transcription factor AP-4 [Source:HGNC Symbol;Acc:HGNC:11745]

Gene Synonyms

AP-4, BHLHC41

Location
About this transcript

This transcript has 7 exons, is annotated with 20 domains and features, is associated with 8672 variant alleles and maps to 523 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000204517.11TFAP4-2012163338aaENSP00000204517.6
 
Protein coding
CCDS10510Q01664 NM_003223.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000572393.1TFAP4-202507115aaENSP00000459390.1
 
Protein coding
I3L254 -TSL:3CDS 3' incomplete
ENST00000573476.1TFAP4-203785167aaENSP00000460067.1
 
Nonsense mediated decay
I3L301 -TSL:3
ENST00000574639.1TFAP4-20459544aaENSP00000461352.1
 
Nonsense mediated decay
I3L4L6 -TSL:5
ENST00000575320.1TFAP4-2066491No protein-
 
Retained intron
--TSL:2
ENST00000575672.1TFAP4-2071613No protein-
 
Retained intron
--TSL:NA
ENST00000575300.1TFAP4-2051326No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 7, Coding exons: 7, Transcript length: 2,163 bps, Translation length: 338 residues

MANE

This MANE Select transcript contains ENSP00000204517 and matches to NM_003223.3 and NP_003214.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q01664

CCDS

This transcript is a member of the Human CCDS set: CCDS10510

Transcript Support Level (TSL)

TSL:1

Version

ENST00000204517.11

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.