Human (GRCh38.p14)
Description

solute carrier family 17 member 9 [Source:HGNC Symbol;Acc:HGNC:16192]

Gene Synonyms

C20ORF59, FLJ23412, VNUT

Location
About this transcript

This transcript has 5 exons, is associated with 1833 variant alleles and maps to 296 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000370351.9SLC17A9-2023518436aaENSP00000359376.4
 
Protein coding
CCDS42901Q9BYT1-1 NM_022082.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000370349.7SLC17A9-2012594430aaENSP00000359374.3
 
Protein coding
CCDS77600Q9BYT1-2 -GENCODE basicTSL:1
ENST00000411611.1SLC17A9-203565152aaENSP00000388215.1
 
Protein coding
Q5W197 -TSL:2CDS 3' incomplete
ENST00000488738.5SLC17A9-2073992No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000459704.6SLC17A9-2042015No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000483113.1SLC17A9-2051624No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000487303.1SLC17A9-206507No protein-
 
Protein coding CDS not defined
--TSL:2
Statistics

Exons: 5, Coding exons: 0, Transcript length: 1,624 bps,

Transcript Support Level (TSL)

TSL:3

Version

ENST00000483113.1

Type

Protein coding CDS not defined

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.