Human (GRCh38.p14)
Description

solute carrier family 25 member 15 [Source:HGNC Symbol;Acc:HGNC:10985]

Gene Synonyms

D13S327, HHH, ORC1, ORNT1

Location
About this transcript

This transcript has 7 exons, is annotated with 11 domains and features, is associated with 9544 variant alleles and maps to 608 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000338625.9SLC25A15-2013821301aaENSP00000342267.4
 
Protein coding
CCDS9373Q9Y619 NM_014252.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000707033.1SLC25A15-2053964301aaENSP00000516711.1
 
Protein coding
CCDS9373--GENCODE basicAPPRIS P1
ENST00000417731.5SLC25A15-202468133aaENSP00000415826.1
 
Protein coding
Q5VZD9 -TSL:5CDS 3' incomplete
ENST00000470509.1SLC25A15-20351157aaENSP00000431429.1
 
Nonsense mediated decay
F2Z354 -TSL:5
ENST00000478827.1SLC25A15-2041142No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 7, Coding exons: 6, Transcript length: 3,821 bps, Translation length: 301 residues

MANE

This MANE Select transcript contains ENSP00000342267 and matches to NM_014252.4 and NP_055067.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9Y619

CCDS

This transcript is a member of the Human CCDS set: CCDS9373

Transcript Support Level (TSL)

TSL:1

Version

ENST00000338625.9

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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