Human (GRCh38.p14)
Description

tenascin R [Source:HGNC Symbol;Acc:HGNC:11953]

About this transcript

This transcript has 23 exons, is annotated with 78 domains and features, is associated with 189668 variant alleles and maps to 871 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000367674.7TNR-201127741358aaENSP00000356646.1
 
Protein coding
CCDS1318Q92752-1 NM_003285.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:5
ENST00000713954.1TNR-203120781304aaENSP00000519247.1
 
Protein coding
A0AAQ5BH57 -GENCODE PrimaryGENCODE Basic
ENST00000713977.1TNR-20536431111aaENSP00000519268.1
 
Protein coding
A0AAQ5BHB2 -GENCODE Basic
ENST00000422274.2TNR-202540180aaENSP00000403413.2
 
Protein coding
H0Y668 -TSL:5CDS 5' and 3' incomplete
ENST00000713955.1TNR-20457291202aaENSP00000519248.1
 
Nonsense mediated decay
A0AAQ5BH92 --
ENST00000713978.1TNR-2062987205aaENSP00000519269.1
 
Nonsense mediated decay
A0AAQ5BH84 --
Statistics

Exons: 23, Coding exons: 21, Transcript length: 12,774 bps, Translation length: 1,358 residues

MANE

This MANE Select transcript contains ENSP00000356646 and matches to NM_003285.3 and NP_003276.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q92752

CCDS

This transcript is a member of the Human CCDS set: CCDS1318

Transcript Support Level (TSL)

TSL:5

Version

ENST00000367674.7

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

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.