Human (GRCh38.p14)
Description

solute carrier family 16 member 10 [Source:HGNC Symbol;Acc:HGNC:17027]

Gene Synonyms

MCT10, TAT1

About this transcript

This transcript has 6 exons, is annotated with 27 domains and features, is associated with 55177 variant alleles and maps to 521 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000368851.10SLC16A10-20210757515aaENSP00000357844.4
 
Protein coding
CCDS5089Q8TF71 NM_018593.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000368850.4SLC16A10-20110051201aaENSP00000357843.1
 
Protein coding
Q9P1I2 -GENCODE basicTSL:1
ENST00000419619.2SLC16A10-203912211aaENSP00000399601.1
 
Protein coding
H0Y5M8 -TSL:3CDS 5' incomplete
ENST00000439288.5SLC16A10-204646206aaENSP00000387501.1
 
Protein coding
H0Y3W8 -TSL:2CDS 5' incomplete
ENST00000465319.1SLC16A10-205734No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 6, Coding exons: 6, Transcript length: 10,757 bps, Translation length: 515 residues

MANE

This MANE Select transcript contains ENSP00000357844 and matches to NM_018593.5 and NP_061063.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8TF71

CCDS

This transcript is a member of the Human CCDS set: CCDS5089

Transcript Support Level (TSL)

TSL:1

Version

ENST00000368851.10

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.