Human (GRCh38.p14)
Description

general transcription factor IIF subunit 2 [Source:HGNC Symbol;Acc:HGNC:4653]

Gene Synonyms

BTF4, RAP30, TFIIF

Location
About this transcript

This transcript has 8 exons, is annotated with 46 domains and features, is associated with 70660 variant alleles and maps to 426 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000340473.8GTF2F2-2012228249aaENSP00000340823.6
 
Protein coding
CCDS9395A0A024RDU9 P13984 NM_004128.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000706694.1GTF2F2-204114777aaENSP00000516507.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000494087.5GTF2F2-2031352No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000706696.1GTF2F2-2061230No protein-
 
Protein coding CDS not defined
---
ENST00000706695.1GTF2F2-2051030No protein-
 
Protein coding CDS not defined
---
ENST00000461904.1GTF2F2-202542No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000706697.1GTF2F2-2071006No protein-
 
Retained intron
---
Statistics

Exons: 8, Coding exons: 8, Transcript length: 2,228 bps, Translation length: 249 residues

MANE

This MANE Select transcript contains ENSP00000340823 and matches to NM_004128.3 and NP_004119.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P13984

CCDS

This transcript is a member of the Human CCDS set: CCDS9395

Transcript Support Level (TSL)

TSL:1

Version

ENST00000340473.8

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.