Human (GRCh38.p14)
Description

transcription factor like 5 [Source:HGNC Symbol;Acc:HGNC:11646]

Gene Synonyms

BHLHE82, CHA, E2BP-1, FIGLB

Location
About this transcript

This transcript has 6 exons, is annotated with 20 domains and features, is associated with 11580 variant alleles and maps to 335 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000335351.8TCFL5-2022625500aaENSP00000334294.3
 
Protein coding
CCDS13506Q9UL49-3 NM_006602.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS ALT2TSL:1
ENST00000895007.1TCFL5-2032514499aaENSP00000565066.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT2
ENST00000217162.5TCFL5-2012453483aaENSP00000217162.5
 
Protein coding
F8W9A4 -GENCODE BasicAPPRIS P4TSL:1
ENST00000895008.1TCFL5-2041967317aaENSP00000565067.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000949323.1TCFL5-2051887449aaENSP00000619382.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT2
Statistics

Exons: 6, Coding exons: 6, Transcript length: 2,625 bps, Translation length: 500 residues

MANE

This MANE Select transcript contains ENSP00000334294 and matches to NM_006602.4 and NP_006593.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UL49

CCDS

This transcript is a member of the Human CCDS set: CCDS13506

Transcript Support Level (TSL)

TSL:1

Version

ENST00000335351.8

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.