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Human (GRCh38.p14)
Description

solute carrier family 12 member 3 [Source:HGNC Symbol;Acc:HGNC:10912]

Gene Synonyms

NCC, NCCT, TSC

Location

Chromosome 16: 56,865,203-56,915,850 forward strand.

GRCh38:CM000678.2

About this gene

This gene has 30 transcripts (splice variants), 204 orthologues, 8 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000563236.6SLC12A3-20355401021aaENSP00000456149.2
 
Protein coding
CCDS58464P55017-1 NM_001126108.2MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00001138971.1SLC12A3-23055441021aaENSP00000814193.1
 
Protein coding
CCDS58464--Ensembl Canonical ExtendedGENCODE Basic
ENST00000898227.2SLC12A3-22757331084aaENSP00000568286.1
 
Protein coding
--GENCODE Basic
ENST00000898208.2SLC12A3-20856581059aaENSP00000568267.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000898207.2SLC12A3-20756491056aaENSP00000568266.1
 
Protein coding
--GENCODE Basic
ENST00000898218.2SLC12A3-21856461055aaENSP00000568277.1
 
Protein coding
--GENCODE Basic
ENST00000438926.7SLC12A3-20255711030aaENSP00000402152.2
 
Protein coding
CCDS10770P55017-2 -GENCODE BasicAPPRIS ALT1TSL:1
ENST00000898221.2SLC12A3-22155591026aaENSP00000568280.1
 
Protein coding
--GENCODE Basic
ENST00000262502.6SLC12A3-20155411020aaENSP00000262502.5
 
Protein coding
CCDS92165J3QSS1 -GENCODE BasicTSL:5
ENST00000898220.2SLC12A3-22055291016aaENSP00000568279.1
 
Protein coding
--GENCODE Basic
ENST00000898226.2SLC12A3-22654901003aaENSP00000568285.1
 
Protein coding
--GENCODE Basic
ENST00000898219.2SLC12A3-2195472997aaENSP00000568278.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000898215.2SLC12A3-2155469996aaENSP00000568274.1
 
Protein coding
--GENCODE Basic
ENST00000898213.2SLC12A3-2135466995aaENSP00000568272.1
 
Protein coding
--GENCODE Basic
ENST00000898214.2SLC12A3-2145448989aaENSP00000568273.1
 
Protein coding
--GENCODE Basic
ENST00000898217.2SLC12A3-2175445988aaENSP00000568276.1
 
Protein coding
--GENCODE Basic
ENST00000898210.2SLC12A3-2105442987aaENSP00000568269.1
 
Protein coding
--GENCODE Basic
ENST00000898224.2SLC12A3-2245439986aaENSP00000568283.1
 
Protein coding
--GENCODE Basic
ENST00000898209.2SLC12A3-2095436985aaENSP00000568268.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000898222.2SLC12A3-2225388969aaENSP00000568281.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000898216.2SLC12A3-2165385968aaENSP00000568275.1
 
Protein coding
--GENCODE Basic
ENST00000898225.2SLC12A3-2255328949aaENSP00000568284.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000898223.2SLC12A3-2235325948aaENSP00000568282.1
 
Protein coding
--GENCODE Basic
ENST00000898212.2SLC12A3-2125298939aaENSP00000568271.1
 
Protein coding
--GENCODE Basic
ENST00000898211.2SLC12A3-2114629716aaENSP00000568270.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000566786.5SLC12A3-20531191029aaENSP00000457552.1
 
Protein coding
CCDS45491P55017-3 -GENCODE BasicAPPRIS P4TSL:1
ENST00000978645.1SLC12A3-229434599aaENSP00000648462.1
 
Nonsense mediated decay
---
ENST00000978644.1SLC12A3-2284291170aaENSP00000648461.1
 
Nonsense mediated decay
---
ENST00000563352.1SLC12A3-204787No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000569002.1SLC12A3-206745No protein-
 
Retained intron
--TSL:2