Human (GRCh37.p13)
Description

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

Gene Synonyms

CTS9

About this transcript

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

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000374016.1DEC1-001125170aaENSP00000363128.1
 
Protein coding
CCDS6812Q9P2X7 NM_017418.2GENCODE basic
ENST00000477580.1DEC1-0032656No protein-
 
Processed transcript
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ENST00000484171.1DEC1-0021208No protein-
 
Processed transcript
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Statistics

Exons: 8, Coding exons: 4, Transcript length: 1,251 bps, Translation length: 70 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9P2X7

CCDS

This transcript is a member of the Human CCDS set: CCDS6812

Version

ENST00000374016.1

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.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000053791 (version 1)
GENCODE basic gene

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