Human (GRCh38.p14)
Description

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

Gene Synonyms

NHE, SLC9A10

Location

Chromosome 3: 112,140,898-112,294,227 reverse strand.

GRCh38:CM000665.2

View alleles of this gene on alternative sequences

About this gene

This gene has 5 transcripts (splice variants), 1 gene allele, 117 orthologues and 10 paralogues.

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