Human (GRCh38.p14)
Description

claudin 14 [Source:HGNC Symbol;Acc:HGNC:2035]

Gene Synonyms

DFNB29

Location
About this transcript

This transcript has 2 exons, is annotated with 20 domains and features, is associated with 8331 variant alleles and maps to 224 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000399135.6CLDN14-2021784239aaENSP00000382087.1
 
Protein coding
CCDS13645O95500 NM_001146079.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000399137.5CLDN14-2041942239aaENSP00000382090.1
 
Protein coding
CCDS13645O95500 -GENCODE basicAPPRIS P1TSL:1
ENST00000342108.2CLDN14-2011453239aaENSP00000339292.2
 
Protein coding
CCDS13645O95500 -GENCODE basicAPPRIS P1TSL:1
ENST00000399136.5CLDN14-2031330239aaENSP00000382088.1
 
Protein coding
CCDS13645O95500 -GENCODE basicAPPRIS P1TSL:1
ENST00000399139.5CLDN14-2051231239aaENSP00000382092.1
 
Protein coding
CCDS13645O95500 -GENCODE basicAPPRIS P1TSL:1
Statistics

Exons: 2, Coding exons: 1, Transcript length: 1,784 bps, Translation length: 239 residues

MANE

This MANE Select transcript contains ENSP00000382087 and matches to NM_001146079.2 and NP_001139551.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: O95500

CCDS

This transcript is a member of the Human CCDS set: CCDS13645

Transcript Support Level (TSL)

TSL:1

Version

ENST00000399135.6

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.