Human (GRCh38.p14)
Description

solute carrier family 9 member A5 [Source:HGNC Symbol;Acc:HGNC:11078]

Gene Synonyms

NHE5

Location

Chromosome 16: 67,237,683-67,272,191 forward strand.

GRCh38:CM000678.2

About this gene

This gene has 9 transcripts (splice variants), 186 orthologues and 10 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000299798.16SLC9A5-2013708896aaENSP00000299798.11
 
Protein coding
CCDS42178Q14940 NM_004594.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000566345.6SLC9A5-206920171aaENSP00000462446.1
 
Protein coding
J3KSE2 -TSL:5CDS 3' incomplete
ENST00000566626.1SLC9A5-207819273aaENSP00000462404.1
 
Protein coding
J3KSB3 -TSL:3CDS 5' and 3' incomplete
ENST00000567247.6SLC9A5-209535178aaENSP00000464393.1
 
Protein coding
J3QRV1 -TSL:3CDS 5' and 3' incomplete
ENST00000564812.5SLC9A5-2053472175aaENSP00000455058.1
 
Nonsense mediated decay
H3BNY2 -TSL:1
ENST00000561472.2SLC9A5-202568No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000564704.5SLC9A5-2044617No protein-
 
Retained intron
--TSL:1
ENST00000563723.5SLC9A5-2033990No protein-
 
Retained intron
--TSL:1
ENST00000566638.1SLC9A5-208704No protein-
 
Retained intron
--TSL:5