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 29 exons, is annotated with 29 domains and features, is associated with 65999 variant alleles and maps to 720 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: 29, Coding exons: 28, Transcript length: 4,119 bps, Translation length: 1,177 residues

MANE

This MANE Select transcript contains ENSP00000306627 and matches to NM_183061.3 and NP_898884.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q4G0N8

CCDS

This transcript is a member of the Human CCDS set: CCDS33817

Transcript Support Level (TSL)

TSL:2

Version

ENST00000305815.10

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.