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 10 exons, is associated with 3311 variant alleles and maps to 392 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: 10, Coding exons: 0, Transcript length: 2,015 bps,

Transcript Support Level (TSL)

TSL:3

Version

ENST00000459704.6

Type

Protein coding CDS not defined

Annotation Method

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