Human (GRCh37.p13)
Description

epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) [Source:HGNC Symbol;Acc:3413]

Gene Synonyms

EPM2, LD, LDE, MELF

About this transcript

This transcript has 2 exons, is associated with 15021 variant alleles and maps to 105 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000367519.3EPM2A-0023633331aaENSP00000356489.3
 
Protein coding
CCDS5206H0UI04 O95278 NM_005670.3Ensembl CanonicalGENCODE basic
ENST00000435470.1EPM2A-0041037237aaENSP00000405913.1
 
Protein coding
--CDS 5' incomplete
ENST00000450221.1EPM2A-001736170aaENSP00000414900.1
 
Protein coding
--CDS 5' incomplete
ENST00000496228.1EPM2A-005781No protein-
 
Processed transcript
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ENST00000461700.1EPM2A-003555No protein-
 
Processed transcript
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ENST00000489412.1EPM2A-006497No protein-
 
Processed transcript
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Statistics

Exons: 2, Coding exons: 0, Transcript length: 497 bps,

Version

ENST00000489412.1

Type

Processed transcript

Annotation Method

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

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000042568 (version 1)