Human (GRCh38.p14)
Description

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

Location
About this transcript

This transcript has 2 exons, is associated with 3423 variant alleles and maps to 86 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: 2, Coding exons: 0, Transcript length: 583 bps,

Transcript Support Level (TSL)

TSL:3

Version

ENST00000496051.1

Type

Protein coding CDS not defined

Annotation Method

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