Human (GRCh38.p14)
Description

tenascin N [Source:HGNC Symbol;Acc:HGNC:22942]

Gene Synonyms

TNW

About this transcript

This transcript has 19 exons, is annotated with 86 domains and features, is associated with 37090 variant alleles and maps to 655 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000239462.9TNN-20150421299aaENSP00000239462.4
 
Protein coding
CCDS30943Q9UQP3 NM_022093.2MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:2
ENST00000860455.1TNN-20456961299aaENSP00000530514.1
 
Protein coding
CCDS30943--GENCODE BasicAPPRIS P1
ENST00000860454.1TNN-20348261122aaENSP00000530513.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000621086.1TNN-20242341122aaENSP00000480895.1
 
Protein coding
A0A087WXC4 -GENCODE PrimaryGENCODE BasicTSL:5
ENST00000946425.1TNN-20541351299aaENSP00000616484.1
 
Protein coding
CCDS30943--GENCODE BasicAPPRIS P1
Statistics

Exons: 19, Coding exons: 18, Transcript length: 5,042 bps, Translation length: 1,299 residues

MANE

This MANE Select transcript contains ENSP00000239462 and matches to NM_022093.2 and NP_071376.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UQP3

CCDS

This transcript is a member of the Human CCDS set: CCDS30943

Transcript Support Level (TSL)

TSL:2

Version

ENST00000239462.9

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.

GENCODE primary gene

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