Human (GRCh38.p14)
Description

solute carrier family 17 member 3 [Source:HGNC Symbol;Acc:HGNC:10931]

Gene Synonyms

NPT4

Location
About this transcript

This transcript has 12 exons, is annotated with 21 domains and features, is associated with 11701 variant alleles and maps to 410 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000397060.8SLC17A3-2042052498aaENSP00000380250.4
 
Protein coding
CCDS47385O00476-2 NM_001098486.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000360657.7SLC17A3-2021750420aaENSP00000353873.3
 
Protein coding
CCDS4566O00476-1 -GENCODE basicTSL:2
ENST00000361703.10SLC17A3-2031543420aaENSP00000355307.6
 
Protein coding
CCDS4566O00476-1 -GENCODE basicTSL:1
ENST00000505420.5SLC17A3-20866151aaENSP00000424027.1
 
Protein coding
H0Y9F7 -TSL:5CDS 5' incomplete
ENST00000481949.6SLC17A3-20659999aaENSP00000421855.1
 
Protein coding
H0Y8R7 -TSL:3CDS 5' incomplete
ENST00000506105.5SLC17A3-2091362112aaENSP00000424729.1
 
Nonsense mediated decay
E9PBQ8 -TSL:2
ENST00000449356.2SLC17A3-205563112aaENSP00000415622.2
 
Nonsense mediated decay
E9PBQ8 -TSL:4
ENST00000509714.5SLC17A3-2101549No protein-
 
Retained intron
--TSL:2
ENST00000503922.5SLC17A3-2071145No protein-
 
Retained intron
--TSL:2
ENST00000308453.5SLC17A3-2011138No protein-
 
Retained intron
--TSL:2

Protein domains for ENSP00000355307.6