Human (GRCh38.p14)
Description

solute carrier family 9 member C1 [Source:HGNC Symbol;Acc:HGNC:31401]

Gene Synonyms

NHE, SLC9A10

About this transcript

This transcript has 28 exons, is annotated with 25 domains and features, is associated with 66007 variant alleles and maps to 597 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000305815.10SLC9C1-20141191177aaENSP00000306627.5
 
Protein coding
CCDS33817Q4G0N8-1 NM_183061.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000487372.5SLC9C1-20539791129aaENSP00000420688.1
 
Protein coding
CCDS82818Q4G0N8-2 -GENCODE basicTSL:1
ENST00000486574.5SLC9C1-20452185aaENSP00000417274.1
 
Protein coding
C9J3M6 -TSL:4CDS 3' incomplete
ENST00000471295.1SLC9C1-2032733241aaENSP00000418371.1
 
Nonsense mediated decay
F8WCJ0 -TSL:5
ENST00000467397.2SLC9C1-20290164aaENSP00000518751.1
 
Nonsense mediated decay
--TSL:4
Statistics

Exons: 28, Coding exons: 27, Transcript length: 3,979 bps, Translation length: 1,129 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q4G0N8

CCDS

This transcript is a member of the Human CCDS set: CCDS82818

Transcript Support Level (TSL)

TSL:1

Version

ENST00000487372.5

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.