Human (GRCh38.p14)
Description

proline rich 27 [Source:HGNC Symbol;Acc:HGNC:33193]

Gene Synonyms

C4ORF40

Location
About this transcript

This transcript has 5 exons, is annotated with 12 domains and features, is associated with 6098 variant alleles and maps to 296 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000344526.10PRR27-2014747219aaENSP00000343172.5
 
Protein coding
CCDS3535Q6MZM9 NM_214711.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000502294.5PRR27-2023007219aaENSP00000426249.1
 
Protein coding
CCDS3535Q6MZM9 -GENCODE BasicAPPRIS P1TSL:1
ENST00000509633.1PRR27-204478426aaENSP00000421286.1
 
Nonsense mediated decay
D6RGD6 -TSL:5
ENST00000512173.1PRR27-20564161aaENSP00000421773.1
 
Nonsense mediated decay
H0Y8Q8 -TSL:3CDS 5' incomplete
ENST00000502441.2PRR27-203667No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 5, Coding exons: 4, Transcript length: 4,747 bps, Translation length: 219 residues

MANE

This MANE Select transcript contains ENSP00000343172 and matches to NM_214711.4 and NP_999876.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q6MZM9

CCDS

This transcript is a member of the Human CCDS set: CCDS3535

Transcript Support Level (TSL)

TSL:1

Version

ENST00000344526.10

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.