Human (GRCh38.p14)
Description

regulatory factor X8 [Source:HGNC Symbol;Acc:HGNC:37253]

Gene Synonyms

FLJ42986

About this transcript

This transcript has 12 exons, is annotated with 2 domains and features, is associated with 33720 variant alleles and maps to 362 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000428343.6RFX8-2012140473aaENSP00000401536.1
 
Protein coding
CCDS46376Q6ZV50-3 NM_001145664.2MANE SelectEnsembl CanonicalGENCODE basicTSL:2
ENST00000646893.2RFX8-2061948586aaENSP00000494249.2
 
Protein coding
Q6ZV50-1 -GENCODE basicAPPRIS P1
ENST00000646446.1RFX8-2051942544aaENSP00000494216.1
 
Protein coding
A0A2R8Y560 -GENCODE basic
ENST00000481179.5RFX8-2021907153aaENSP00000422968.1
 
Nonsense mediated decay
E9PDA6 -TSL:2
ENST00000484091.1RFX8-20353080aaENSP00000424661.1
 
Nonsense mediated decay
D6RAX4 -TSL:4
ENST00000492238.1RFX8-204774No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 12, Coding exons: 11, Transcript length: 2,140 bps, Translation length: 473 residues

MANE

This MANE Select transcript contains ENSP00000401536 and matches to NM_001145664.2 and NP_001139136.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q6ZV50

CCDS

This transcript is a member of the Human CCDS set: CCDS46376

Transcript Support Level (TSL)

TSL:2

Version

ENST00000428343.6

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.