Human (GRCh38.p14)
Description

solute carrier family 17 member 5 [Source:HGNC Symbol;Acc:HGNC:10933]

Gene Synonyms

AST, ISSD, NSD, SD, SIALIN, SIASD, SLD

Location

Chromosome 6: 73,593,364-73,654,014 reverse strand.

GRCh38:CM000668.2

About this gene

This gene has 8 transcripts (splice variants), 339 orthologues, 12 paralogues and is associated with 6 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000355773.6SLC17A5-2013292495aaENSP00000348019.5
 
Protein coding
CCDS4981Q9NRA2-1 NM_012434.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000908538.1SLC17A5-2043200466aaENSP00000578597.1
 
Protein coding
--GENCODE Basic
ENST00000957535.1SLC17A5-2073184469aaENSP00000627594.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000908537.1SLC17A5-2033155442aaENSP00000578596.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000933630.1SLC17A5-2053061417aaENSP00000603689.1
 
Protein coding
--GENCODE Basic
ENST00000933631.1SLC17A5-2062903369aaENSP00000603690.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000957536.1SLC17A5-2082761533aaENSP00000627595.1
 
Protein coding
--GENCODE Basic
ENST00000481996.1SLC17A5-202734No protein-
 
Protein coding CDS not defined
--TSL:4