Human (GRCh38.p14)
Description

solute carrier family 12 member 7 [Source:HGNC Symbol;Acc:HGNC:10915]

Gene Synonyms

DKFZP434F076, KCC4

Location

Chromosome 5: 1,050,384-1,112,063 reverse strand.

GRCh38:CM000667.2

View alleles of this gene on alternative sequences

About this gene

This gene has 6 transcripts (splice variants), 1 gene allele, 282 orthologues and 8 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000264930.10SLC12A7-20153001083aaENSP00000264930.5
 
Protein coding
CCDS34129Q9Y666-1 NM_006598.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000634447.1SLC12A7-2063142989aaENSP00000489285.1
 
Protein coding
A0A0U1RR18 -TSL:5CDS 5' incomplete
ENST00000513223.2SLC12A7-2041066355aaENSP00000428854.2
 
Protein coding
H0YB78 -TSL:5CDS 5' and 3' incomplete
ENST00000504576.2SLC12A7-20268063aaENSP00000489272.1
 
Nonsense mediated decay
A0A0U1RR10 -TSL:5CDS 5' incomplete
ENST00000514994.1SLC12A7-205586No protein-
 
Retained intron
--TSL:3
ENST00000510943.3SLC12A7-203421No protein-
 
Retained intron
--TSL:3