Human (GRCh38.p14)
Description

serine and arginine rich splicing factor 6 [Source:HGNC Symbol;Acc:HGNC:10788]

Gene Synonyms

B52, SFRS6, SRP55

Location
About this transcript

This transcript has 6 exons, is annotated with 22 domains and features, is associated with 4453 variant alleles and maps to 543 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000244020.5SRSF6-2014353344aaENSP00000244020.3
 
Protein coding
CCDS13318Q13247-1 NM_006275.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000668808.1SRSF6-2041227276aaENSP00000499517.1
 
Protein coding
A0A590UJP7 -GENCODE basicAPPRIS ALT2
ENST00000670741.1SRSF6-2051077226aaENSP00000499492.1
 
Protein coding
A0A590UJK4 -GENCODE basicAPPRIS ALT2
ENST00000662078.1SRSF6-2031007273aaENSP00000499666.1
 
Protein coding
A0A590UK01 -GENCODE basicAPPRIS ALT2
ENST00000483871.6SRSF6-2021680135aaENSP00000433544.1
 
Nonsense mediated decay
Q13247-2 -TSL:2
ENST00000671022.1SRSF6-2061275No protein-
 
Protein coding CDS not defined
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Statistics

Exons: 6, Coding exons: 6, Transcript length: 4,353 bps, Translation length: 344 residues

MANE

This MANE Select transcript contains ENSP00000244020 and matches to NM_006275.6 and NP_006266.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q13247

CCDS

This transcript is a member of the Human CCDS set: CCDS13318

Transcript Support Level (TSL)

TSL:1

Version

ENST00000244020.5

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.