Human (GRCh38.p14)
Description

clarin 3 [Source:HGNC Symbol;Acc:HGNC:20795]

Gene Synonyms

MGC32871, TMEM12, USH3AL1

About this transcript

This transcript has 3 exons, is annotated with 19 domains and features, is associated with 6895 variant alleles and maps to 222 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000368671.4CLRN3-2011146226aaENSP00000357660.3
 
Protein coding
CCDS7656Q8NCR9-1 NM_152311.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P3TSL:1
ENST00000856090.1CLRN3-2041147230aaENSP00000526149.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT1
ENST00000856089.1CLRN3-2031134225aaENSP00000526148.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT1
ENST00000856091.1CLRN3-2051111224aaENSP00000526150.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT1
ENST00000856088.1CLRN3-202970166aaENSP00000526147.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
Statistics

Exons: 3, Coding exons: 3, Transcript length: 1,146 bps, Translation length: 226 residues

MANE

This MANE Select transcript contains ENSP00000357660 and matches to NM_152311.5 and NP_689524.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8NCR9

CCDS

This transcript is a member of the Human CCDS set: CCDS7656

Transcript Support Level (TSL)

TSL:1

Version

ENST00000368671.4

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.

GENCODE primary gene

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