Human (GRCh38.p14)
Description

family with sequence similarity 216 member A [Source:HGNC Symbol;Acc:HGNC:30180]

Gene Synonyms

C12ORF24, HSU79274

About this transcript

This transcript has 7 exons, is annotated with 7 domains and features, is associated with 9434 variant alleles and maps to 326 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000377673.10FAM216A-2011101273aaENSP00000366901.5
 
Protein coding
CCDS31899Q8WUB2 NM_013300.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000548449.1FAM216A-20592977aaENSP00000448777.1
 
Nonsense mediated decay
F8VXY8 -TSL:1
ENST00000538285.6FAM216A-2021679No protein-
 
Retained intron
--TSL:1
ENST00000547539.1FAM216A-2041384No protein-
 
Retained intron
--TSL:2
ENST00000548869.1FAM216A-2061160No protein-
 
Retained intron
--TSL:2
ENST00000546396.1FAM216A-203792No protein-
 
Retained intron
--TSL:5
Statistics

Exons: 7, Coding exons: 7, Transcript length: 1,101 bps, Translation length: 273 residues

MANE

This MANE Select transcript contains ENSP00000366901 and matches to NM_013300.3 and NP_037432.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8WUB2

CCDS

This transcript is a member of the Human CCDS set: CCDS31899

Transcript Support Level (TSL)

TSL:1

Version

ENST00000377673.10

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.