Human (GRCh38.p14)
Description

novel transcript

Location
About this transcript

This transcript has 17 exons, is associated with 11558 variant alleles and maps to 1634 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000480319.5-3872No protein-
 
Retained intron
-TSL:2
ENST00000486209.5-3213No protein-
 
Retained intron
-TSL:5
ENST00000463608.5-2816No protein-
 
Retained intron
-TSL:5
ENST00000462560.6-2553No protein-
 
Retained intron
-TSL:1
ENST00000470274.5-2414No protein-
 
Retained intron
-TSL:2
ENST00000494740.5-2273No protein-
 
Retained intron
-TSL:5
ENST00000479693.1-1906No protein-
 
Retained intron
-TSL:1
ENST00000467443.5-1869No protein-
 
Retained intron
-TSL:2
ENST00000477296.5-1787No protein-
 
Retained intron
-TSL:2
ENST00000476537.1-276No protein-
 
Retained intron
-TSL:2
ENST00000491562.5-209No protein-
 
Retained intron
-TSL:5
ENST00000450651.5-2294No protein-
 
lncRNA
-Ensembl CanonicalGENCODE basicTSL:5
Statistics

Exons: 17, Coding exons: 0, Transcript length: 2,294 bps,

Transcript Support Level (TSL)

TSL:5

Version

ENST00000450651.5

Type

LncRNA

Annotation Method

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

Annotation Attributes

overlaps pseudogene [Definitions]

GENCODE basic gene

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