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 2 exons, is associated with 1281 variant alleles and maps to 80 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: 2, Coding exons: 0, Transcript length: 745 bps,

Transcript Support Level (TSL)

TSL:2

Version

ENST00000569002.1

Type

Retained intron

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.