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Human (GRCh38.p14)
Description

myocyte enhancer factor 2D [Source:HGNC Symbol;Acc:HGNC:6997]

About this transcript

This transcript has 11 exons, is annotated with 23 domains and features, is associated with 11078 variant alleles and maps to 566 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000348159.9MEF2D-2015912521aaENSP00000271555.5
 
Protein coding
CCDS1143Q14814-1 NM_005920.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000464356.6MEF2D-2035598513aaENSP00000476788.1
 
Protein coding
Q14814-5 -GENCODE PrimaryGENCODE BasicAPPRIS P1TSL:5
ENST00000360595.7MEF2D-2023194514aaENSP00000353803.3
 
Protein coding
CCDS60304Q14814-4 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000489057.1MEF2D-20559310aaENSP00000477124.1
 
Protein coding
A0A0G2JLL8 -TSL:5CDS 3' incomplete
ENST00000475587.2MEF2D-2041627139aaENSP00000477413.1
 
Nonsense mediated decay
Q05BX2 -TSL:5
ENST00000493077.1MEF2D-206526No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 11, Coding exons: 10, Transcript length: 3,194 bps, Translation length: 514 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q14814

CCDS

This transcript is a member of the Human CCDS set: CCDS60304

Transcript Support Level (TSL)

TSL:1

Version

ENST00000360595.7

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.