Human (GRCh38.p14)
Description

spermatogenesis associated 9 [Source:HGNC Symbol;Acc:HGNC:22988]

Gene Synonyms

FLJ35906, NYD-SP16

Location
About this transcript

This transcript has 5 exons, is annotated with 5 domains and features, is associated with 9391 variant alleles and maps to 312 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000274432.13SPATA9-2011210254aaENSP00000274432.8
 
Protein coding
CCDS4076Q9BWV2-1 NM_031952.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000477715.5SPATA9-2052169178aaENSP00000427257.1
 
Nonsense mediated decay
Q9BWV2-2 -TSL:2
ENST00000316087.12SPATA9-2021583254aaENSP00000325491.8
 
Nonsense mediated decay
CCDS4076Q9BWV2-1 -TSL:1
ENST00000489917.1SPATA9-2061046135aaENSP00000420883.1
 
Nonsense mediated decay
Q9BWV2-3 -TSL:1
ENST00000477047.6SPATA9-2041592No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000379990.9SPATA9-203702No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 5, Coding exons: 5, Transcript length: 1,210 bps, Translation length: 254 residues

MANE

This MANE Select transcript contains ENSP00000274432 and matches to NM_031952.4 and NP_114158.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9BWV2

CCDS

This transcript is a member of the Human CCDS set: CCDS4076

Transcript Support Level (TSL)

TSL:1

Version

ENST00000274432.13

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.