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 9648 variant alleles and maps to 628 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: 3,964 bps, Translation length: 301 residues

CCDS

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

Version

ENST00000707033.1

Type

Protein coding

Annotation Method

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

Annotation Attributes

RNA-Seq supported only [Definitions]

GENCODE basic gene

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