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Human (GRCh38.p14)
Description

ring finger protein 126 [Source:HGNC Symbol;Acc:HGNC:21151]

Gene Synonyms

FLJ20552

Location
About this transcript

This transcript has 9 exons, is annotated with 19 domains and features, is associated with 10441 variant alleles and maps to 573 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000292363.10RNF126-2011631311aaENSP00000292363.3
 
Protein coding
CCDS12039Q9BV68 NM_194460.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000589762.5RNF126-203963283aaENSP00000464945.2
 
Protein coding
K7EIY6 -TSL:2CDS 3' incomplete
ENST00000605891.5RNF126-207167174aaENSP00000475833.1
 
Nonsense mediated decay
U3KQF4 -TSL:5
ENST00000590885.6RNF126-2041436No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000586749.1RNF126-2022092No protein-
 
Retained intron
--TSL:2
ENST00000591394.2RNF126-205733No protein-
 
Retained intron
--TSL:2
ENST00000592626.3RNF126-206652No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 9, Coding exons: 9, Transcript length: 1,631 bps, Translation length: 311 residues

MANE

This MANE Select transcript contains ENSP00000292363 and matches to NM_194460.3 and NP_919442.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9BV68

CCDS

This transcript is a member of the Human CCDS set: CCDS12039

Transcript Support Level (TSL)

TSL:1

Version

ENST00000292363.10

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.