Human (GRCh38.p14)
Description

serine incorporator 5 [Source:HGNC Symbol;Acc:HGNC:18825]

Gene Synonyms

C5ORF12, TPO1

Location
About this transcript

This transcript has 12 exons, is annotated with 14 domains and features, is associated with 55314 variant alleles and maps to 473 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000507668.7SERINC5-2026448461aaENSP00000426237.3
 
Protein coding
CCDS54874Q86VE9-4 NM_001174072.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000509193.5SERINC5-2031441420aaENSP00000426134.2
 
Protein coding
CCDS83009Q86VE9-2 -GENCODE basicTSL:1
ENST00000512972.6SERINC5-2041627417aaENSP00000421665.2
 
Nonsense mediated decay
Q86VE9-3 -TSL:2
ENST00000632581.1SERINC5-2061573456aaENSP00000488864.1
 
Nonsense mediated decay
A0A0J9YYI4 -TSL:2
ENST00000513907.1SERINC5-205547No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000502747.1SERINC5-2012767No protein-
 
Retained intron
--TSL:1
Statistics

Exons: 12, Coding exons: 12, Transcript length: 6,448 bps, Translation length: 461 residues

MANE

This MANE Select transcript contains ENSP00000426237 and matches to NM_001174072.3 and NP_001167543.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q86VE9

CCDS

This transcript is a member of the Human CCDS set: CCDS54874

Transcript Support Level (TSL)

TSL:2

Version

ENST00000507668.7

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.