Human (GRCh38.p14)
Description

solute carrier family 35 member B3 [Source:HGNC Symbol;Acc:HGNC:21601]

Gene Synonyms

C6ORF196, CGI-19, DJ453H5.1, PAPST2

Location
About this transcript

This transcript has 11 exons, is annotated with 13 domains and features, is associated with 9029 variant alleles and maps to 441 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000710437.1SLC35B3-2063520369aaENSP00000518269.1
 
Protein coding
CCDS93854-NM_001370479.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1
ENST00000644923.2SLC35B3-2023566401aaENSP00000496368.1
 
Protein coding
CCDS4508Q9H1N7-1 -GENCODE basic
ENST00000379660.4SLC35B3-2012137401aaENSP00000368981.4
 
Protein coding
CCDS4508Q9H1N7-1 -GENCODE basicTSL:1
ENST00000648987.1SLC35B3-2041911369aaENSP00000498054.1
 
Protein coding
CCDS93854A0A024QZW4 -GENCODE basicAPPRIS P1
ENST00000649788.1SLC35B3-2052442251aaENSP00000496851.1
 
Nonsense mediated decay
A0A3B3IRN3 --
ENST00000648867.1SLC35B3-2032200283aaENSP00000497645.1
 
Nonsense mediated decay
Q9H1N7-3 --
Statistics

Exons: 11, Coding exons: 10, Transcript length: 2,137 bps, Translation length: 401 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9H1N7

CCDS

This transcript is a member of the Human CCDS set: CCDS4508

Transcript Support Level (TSL)

TSL:1

Version

ENST00000379660.4

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.