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Human (GRCh38.p14)
Description

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

Gene Synonyms

DKFZP434F076, KCC4

Location

Scaffold HSCHR5_4_CTG1: 68,885-129,717 reverse strand.

GRCh38:KI270792.1

View this gene on the primary assembly.

About this gene

This gene has 5 transcripts (splice variants) and 1 gene allele.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000611005.3SLC12A7-21152801083aaENSP00000482242.1
 
Protein coding
A0A0G2JNW7 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000628680.1SLC12A7-2141041347aaENSP00000485792.1
 
Protein coding
A0A0G2JQE3 -TSL:3CDS 5' and 3' incomplete
ENST00000629404.1SLC12A7-215661No protein-
 
Retained intron
--TSL:3
ENST00000627842.1SLC12A7-213586No protein-
 
Retained intron
--TSL:3
ENST00000625568.1SLC12A7-212421No protein-
 
Retained intron
--TSL:3