Human (GRCh38.p14)
Description

deleted in esophageal cancer 1 [Source:HGNC Symbol;Acc:HGNC:23658]

Gene Synonyms

CTS9, DEC1

About this transcript

This transcript has 8 exons, is associated with 112487 variant alleles and maps to 333 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000649121.1DELEC1-2081064No protein-
 
lncRNA
-Ensembl CanonicalGENCODE basic
ENST00000647970.1DELEC1-2052864No protein-
 
lncRNA
-GENCODE basic
ENST00000477580.5DELEC1-2022656No protein-
 
lncRNA
-TSL:2
ENST00000484171.2DELEC1-2031581No protein-
 
lncRNA
-TSL:1
ENST00000374016.5DELEC1-2011251No protein-
 
lncRNA
-GENCODE basicTSL:1
ENST00000649565.1DELEC1-209570No protein-
 
lncRNA
--
ENST00000648852.1DELEC1-207555No protein-
 
lncRNA
-GENCODE basic
ENST00000614246.1DELEC1-204210No protein-
 
lncRNA
-TSL:1
ENST00000647996.1DELEC1-206183No protein-
 
lncRNA
--
Statistics

Exons: 8, Coding exons: 0, Transcript length: 1,251 bps,

Transcript Support Level (TSL)

TSL:1

Version

ENST00000374016.5

Type

LncRNA

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.