Human (GRCh38.p14)
Description

chromosome 11 open reading frame 16 [Source:HGNC Symbol;Acc:HGNC:1169]

Location
About this transcript

This transcript has 7 exons, is annotated with 6 domains and features, is associated with 6128 variant alleles and maps to 326 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000326053.10C11orf16-2011866467aaENSP00000318999.5
 
Protein coding
CCDS7794Q9NQ32-1 NM_020643.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000525780.5C11orf16-2021685404aaENSP00000436818.1
 
Protein coding
Q9NQ32-2 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000528830.3C11orf16-205593128aaENSP00000437069.1
 
Nonsense mediated decay
E9PNY9 -TSL:4
ENST00000528998.5C11orf16-206565No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000526227.3C11orf16-203563No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000527607.1C11orf16-204924No protein-
 
Retained intron
--TSL:4
Statistics

Exons: 7, Coding exons: 5, Transcript length: 1,866 bps, Translation length: 467 residues

MANE

This MANE Select transcript contains ENSP00000318999 and matches to NM_020643.3 and NP_065694.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NQ32

CCDS

This transcript is a member of the Human CCDS set: CCDS7794

Transcript Support Level (TSL)

TSL:1

Version

ENST00000326053.10

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.