Human (GRCh38.p14)
Description

solute carrier family 5 member 7 [Source:HGNC Symbol;Acc:HGNC:14025]

Gene Synonyms

CHT, CHT1, HCHT

Location

Chromosome 2: 107,986,523-108,013,994 forward strand.

GRCh38:CM000664.2

About this gene

This gene has 2 transcripts (splice variants), 286 orthologues, 11 paralogues and is associated with 5 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000264047.3SLC5A7-2015167580aaENSP00000264047.2
 
Protein coding
CCDS2074Q9GZV3 NM_021815.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000409059.5SLC5A7-2022032580aaENSP00000387346.1
 
Protein coding
CCDS2074Q9GZV3 -GENCODE basicAPPRIS P1TSL:1