Human (GRCh38.p14)
Description

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

Gene Synonyms

NHE, SLC9A10

Location

Scaffold HSCHR3_6_CTG2_1: 24,188-186,965 reverse strand.

GRCh38:KZ559105.1

View this gene on the primary assembly.

About this gene

This gene has 5 transcripts (splice variants) and 1 gene allele.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000642317.2SLC9C1-20641191177aaENSP00000495147.1
 
Protein coding
Q4G0N8-1 -Ensembl CanonicalGENCODE basic
ENST00000647463.1SLC9C1-21039791129aaENSP00000495048.1
 
Protein coding
Q4G0N8-2 -GENCODE basic
ENST00000642787.1SLC9C1-20752185aaENSP00000496221.1
 
Protein coding
C9J3M6 -CDS 3' incomplete
ENST00000644496.1SLC9C1-2092733241aaENSP00000494242.1
 
Nonsense mediated decay
F8WCJ0 --
ENST00000643172.2SLC9C1-20890164aaENSP00000518750.1
 
Nonsense mediated decay
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