Human (GRCh37.p13)
Description

desmin [Source:HGNC Symbol;Acc:2770]

Gene Synonyms

CMD1I, CSM1, CSM2, LGMD2R

Location

Chromosome 2: 220,283,099-220,291,461 forward strand.

GRCh37:CM000664.1

About this gene

This gene has 4 transcripts (splice variants), 9 paralogues and is associated with 9 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000373960.3DES-0012248470aaENSP00000363071.3
 
Protein coding
CCDS33383L7R9R4 P17661 Q2PUK1
Q53SB5 Q9GZR6
NM_001927.3Ensembl CanonicalGENCODE Basic
ENST00000477226.1DES-006760No protein-
 
Retained intron
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ENST00000492726.1DES-007706No protein-
 
Retained intron
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ENST00000483395.1DES-008462No protein-
 
Retained intron
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