Human (GRCh38.p14)
Description

solute carrier family 25 member 46 [Source:HGNC Symbol;Acc:HGNC:25198]

Location

Chromosome 5: 110,738,136-110,765,161 forward strand.

GRCh38:CM000667.2

About this gene

This gene has 8 transcripts (splice variants), 214 orthologues and is associated with 5 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000355943.8SLC25A46-2014745418aaENSP00000348211.3
 
Protein coding
CCDS4100Q96AG3-1 NM_138773.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000504098.1SLC25A46-2042345272aaENSP00000425708.1
 
Protein coding
Q96AG3-2 -GENCODE basicTSL:5
ENST00000509432.1SLC25A46-2061596205aaENSP00000426604.1
 
Protein coding
B7Z6C8 -GENCODE basicTSL:2
ENST00000447245.6SLC25A46-2021575337aaENSP00000399717.2
 
Protein coding
CCDS78045Q96AG3-3 -GENCODE basicTSL:2
ENST00000513807.5SLC25A46-2081546256aaENSP00000421134.1
 
Protein coding
E7EVY2 -GENCODE basicTSL:2
ENST00000513706.2SLC25A46-2076236No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000508781.5SLC25A46-205558No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000502462.6SLC25A46-2031446No protein-
 
Retained intron
--TSL:2