Human (GRCh38.p14)
Description

solute carrier family 16 member 14 [Source:HGNC Symbol;Acc:HGNC:26417]

Gene Synonyms

FLJ30794, MCT14

About this transcript

This transcript has 5 exons, is annotated with 19 domains and features, is associated with 14541 variant alleles and maps to 357 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000295190.9SLC16A14-2014315510aaENSP00000295190.4
 
Protein coding
CCDS2473Q7RTX9-1 NM_152527.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000457406.5SLC16A14-2051836489aaENSP00000400352.1
 
Protein coding
E7EMG7 -TSL:1CDS 3' incomplete
ENST00000412034.5SLC16A14-2021672485aaENSP00000395775.1
 
Protein coding
Q6ZWE5 -TSL:2CDS 3' incomplete
ENST00000436869.1SLC16A14-20464618aaENSP00000396834.1
 
Protein coding
C9JIV1 -TSL:4CDS 3' incomplete
ENST00000425822.5SLC16A14-20353742aaENSP00000389726.1
 
Protein coding
C9JME4 -TSL:4CDS 3' incomplete
Statistics

Exons: 5, Coding exons: 4, Transcript length: 4,315 bps, Translation length: 510 residues

MANE

This MANE Select transcript contains ENSP00000295190 and matches to NM_152527.5 and NP_689740.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q7RTX9

CCDS

This transcript is a member of the Human CCDS set: CCDS2473

Transcript Support Level (TSL)

TSL:1

Version

ENST00000295190.9

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.