Human (GRCh38.p14)
Description

chromosome 16 open reading frame 89 [Source:HGNC Symbol;Acc:HGNC:28687]

Gene Synonyms

MGC45438

Location
About this transcript

This transcript has 8 exons, is annotated with 5 domains and features, is associated with 13090 variant alleles and maps to 289 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000472572.8C16orf89-2021360361aaENSP00000420566.2
 
Protein coding
CCDS45404Q6UX73-2 NM_001098514.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000315997.5C16orf89-2011872402aaENSP00000324672.5
 
Protein coding
CCDS42116Q6UX73-1 -GENCODE basicTSL:1
ENST00000474471.7C16orf89-2031829434aaENSP00000417158.3
 
Protein coding
A0A0A0MT71 -GENCODE basicTSL:5
ENST00000591875.1C16orf89-205582No protein-
 
Retained intron
--TSL:2
ENST00000586629.5C16orf89-204576No protein-
 
Retained intron
--TSL:2
ENST00000592343.1C16orf89-206456No protein-
 
Retained intron
--TSL:5
Statistics

Exons: 8, Coding exons: 8, Transcript length: 1,360 bps, Translation length: 361 residues

MANE

This MANE Select transcript contains ENSP00000420566 and matches to NM_001098514.3 and NP_001091984.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q6UX73

CCDS

This transcript is a member of the Human CCDS set: CCDS45404

Transcript Support Level (TSL)

TSL:1

Version

ENST00000472572.8

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Annotation Attributes

upstream ATG [Definitions]

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.