Human (GRCh38.p14)
Description

solute carrier family 25 member 30 [Source:HGNC Symbol;Acc:HGNC:27371]

Location

Chromosome 13: 45,393,316-45,418,455 reverse strand.

GRCh38:CM000675.2

About this gene

This gene has 8 transcripts (splice variants), 181 orthologues and 49 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000519676.6SLC25A30-2043663291aaENSP00000429168.1
 
Protein coding
CCDS31967Q5SVS4-1 NM_001010875.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000539591.5SLC25A30-2073608240aaENSP00000443542.1
 
Protein coding
CCDS66539Q5SVS4-2 -GENCODE basicTSL:2
ENST00000519547.5SLC25A30-203582137aaENSP00000429308.1
 
Protein coding
E5RIW6 -TSL:4CDS 3' incomplete
ENST00000618165.1SLC25A30-208525119aaENSP00000480455.1
 
Protein coding
A0A087WWR9 -TSL:3CDS 5' incomplete
ENST00000522438.1SLC25A30-20545394aaENSP00000430687.1
 
Protein coding
E5RIS9 -TSL:5CDS 3' incomplete
ENST00000310862.11SLC25A30-201109437aaENSP00000311856.7
 
Nonsense mediated decay
D6RJI0 -TSL:1
ENST00000463262.1SLC25A30-20242637aaENSP00000425603.1
 
Nonsense mediated decay
D6RJI0 -TSL:3
ENST00000523988.5SLC25A30-2066041No protein-
 
Retained intron
--TSL:2