Human (GRCh38.p14)
Description

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

Gene Synonyms

NCC, NCCT, TSC

Location
About this transcript

This transcript has 26 exons, is annotated with 25 domains and features, is associated with 24939 variant alleles and maps to 742 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000563236.6SLC12A3-20355401021aaENSP00000456149.2
 
Protein coding
CCDS58464P55017-1 NM_001126108.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT1TSL:1
ENST00000438926.6SLC12A3-20255671030aaENSP00000402152.2
 
Protein coding
CCDS10770P55017-2 -GENCODE basicAPPRIS ALT1TSL:1
ENST00000262502.5SLC12A3-20142081020aaENSP00000262502.5
 
Protein coding
CCDS92165J3QSS1 -GENCODE basicAPPRIS ALT1TSL:5
ENST00000566786.5SLC12A3-20531191029aaENSP00000457552.1
 
Protein coding
CCDS45491P55017-3 -GENCODE basicAPPRIS P4TSL:1
ENST00000563352.1SLC12A3-204787No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000569002.1SLC12A3-206745No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 26, Coding exons: 26, Transcript length: 5,567 bps, Translation length: 1,030 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P55017

CCDS

This transcript is a member of the Human CCDS set: CCDS10770

Transcript Support Level (TSL)

TSL:1

Version

ENST00000438926.6

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.