Human (GRCh38.p14)
Description

spermatogenesis associated 16 [Source:HGNC Symbol;Acc:HGNC:29935]

Gene Synonyms

NYD-SP12

About this transcript

This transcript has 11 exons, is annotated with 6 domains and features, is associated with 99998 variant alleles and maps to 439 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000351008.4SPATA16-2012074569aaENSP00000341765.3
 
Protein coding
CCDS3221A0A140VJV8 Q9BXB7 NM_031955.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000652082.1SPATA16-2021124214aaENSP00000498213.1
 
Nonsense mediated decay
A0A494BZR9 -CDS 5' incomplete
Statistics

Exons: 11, Coding exons: 10, Transcript length: 2,074 bps, Translation length: 569 residues

MANE

This MANE Select transcript contains ENSP00000341765 and matches to NM_031955.6 and NP_114161.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9BXB7

CCDS

This transcript is a member of the Human CCDS set: CCDS3221

Transcript Support Level (TSL)

TSL:1

Version

ENST00000351008.4

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.