Human (GRCh38.p14)
Description

solute carrier family 25 member 18 [Source:HGNC Symbol;Acc:HGNC:10988]

Location
About this transcript

This transcript has 10 exons, is annotated with 19 domains and features, is associated with 13865 variant alleles and maps to 374 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000327451.11SLC25A18-2012186315aaENSP00000329033.5
 
Protein coding
CCDS13744A0A024R0W0 Q9H1K4 NM_031481.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000399813.1SLC25A18-2022057315aaENSP00000382710.1
 
Protein coding
CCDS13744A0A024R0W0 Q9H1K4 -GENCODE basicAPPRIS P1TSL:1
ENST00000497401.1SLC25A18-206845No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000496051.1SLC25A18-205583No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000469889.1SLC25A18-204560No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000467228.1SLC25A18-2032454No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 10, Coding exons: 9, Transcript length: 2,057 bps, Translation length: 315 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9H1K4

CCDS

This transcript is a member of the Human CCDS set: CCDS13744

Transcript Support Level (TSL)

TSL:1

Version

ENST00000399813.1

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.