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Human (GRCh37.p13)
Description

stimulated by retinoic acid 13 [Source:HGNC Symbol;Acc:11422]

Gene Synonyms

CENP-X, CENPX, D9, FAAP10, MGC14480, MHF2

Location
About this transcript

This transcript has 5 exons, is annotated with 1 domain and feature, is associated with 2549 variant alleles and maps to 249 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000392359.3STRA13-00280581aaENSP00000376168.3
 
Protein coding
CCDS59303A8MT69 NM_001271006.1Ensembl CanonicalGENCODE basic
ENST00000584347.1STRA13-006799131aaENSP00000464357.1
 
Protein coding
J3QRS1 -GENCODE basic
ENST00000306704.6STRA13-00175163aaENSP00000302951.6
 
Protein coding
CCDS32772A8MT69 NM_144998.3GENCODE basic
ENST00000584600.1STRA13-00873075aaENSP00000463974.1
 
Protein coding
J3QR01 -CDS 5' incomplete
ENST00000580435.1STRA13-00371058aaENSP00000462015.1
 
Protein coding
CCDS59302A8MT69 NM_001271007.1GENCODE basic
ENST00000579520.1STRA13-00470266aaENSP00000464024.1
 
Protein coding
--CDS 5' incomplete
ENST00000583767.1STRA13-009894No protein-
 
Processed transcript
---
ENST00000584514.1STRA13-011882No protein-
 
Processed transcript
---
ENST00000577379.1STRA13-010861No protein-
 
Processed transcript
---
ENST00000580090.1STRA13-007752No protein-
 
Processed transcript
---
ENST00000585091.1STRA13-005739No protein-
 
Retained intron
---
Statistics

Exons: 5, Coding exons: 5, Transcript length: 805 bps, Translation length: 81 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: A8MT69

CCDS

This transcript is a member of the Human CCDS set: CCDS59303

Version

ENST00000392359.3

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:
OTTHUMT00000255174 (version 1)
GENCODE basic gene

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