Human (GRCh38.p14)
Description

solute carrier family 25 member 20 [Source:HGNC Symbol;Acc:HGNC:1421]

Gene Synonyms

CAC, CACT

Location
About this transcript

This transcript has 9 exons, is annotated with 15 domains and features, is associated with 17858 variant alleles and maps to 461 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000319017.5SLC25A20-2011778301aaENSP00000326305.4
 
Protein coding
CCDS2779O43772 NM_000387.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000430379.5SLC25A20-2021576228aaENSP00000388986.1
 
Protein coding
C9JPE1 -GENCODE basicTSL:3
ENST00000440964.1SLC25A20-203138376aaENSP00000388563.1
 
Nonsense mediated decay
F8WEF6 -TSL:2
ENST00000479050.1SLC25A20-204694No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 9, Coding exons: 9, Transcript length: 1,778 bps, Translation length: 301 residues

MANE

This MANE Select transcript contains ENSP00000326305 and matches to NM_000387.6 and NP_000378.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: O43772

CCDS

This transcript is a member of the Human CCDS set: CCDS2779

Transcript Support Level (TSL)

TSL:1

Version

ENST00000319017.5

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.