Human (GRCh38.p14)
Description

solute carrier family 26 member 3 [Source:HGNC Symbol;Acc:HGNC:3018]

Gene Synonyms

CLD, DRA

Location

Chromosome 7: 107,765,467-107,803,225 reverse strand.

GRCh38:CM000669.2

About this gene

This gene has 5 transcripts (splice variants), 242 orthologues, 9 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000340010.10SLC26A3-2012882764aaENSP00000345873.5
 
Protein coding
CCDS5748P40879 NM_000111.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000453332.1SLC26A3-203552120aaENSP00000395955.1
 
Protein coding
C9JFJ2 -TSL:4CDS 3' incomplete
ENST00000379083.7SLC26A3-202260252aaENSP00000368375.3
 
Nonsense mediated decay
F8WBL6 -TSL:2
ENST00000469651.1SLC26A3-205646No protein-
 
Retained intron
--TSL:2
ENST00000468551.1SLC26A3-204556No protein-
 
Retained intron
--TSL:2