Human (GRCh37.p13)
Description

dystrophia myotonica, WD repeat containing [Source:HGNC Symbol;Acc:2936]

Gene Synonyms

D19S593E, DM9, DMR-N9, DMRN9, gene59

Location
About this transcript

This transcript has 1 exon, is associated with 420 variant alleles and maps to 23 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000270223.6DMWD-0023305674aaENSP00000270223.5
 
Protein coding
CCDS33054Q09019 NM_004943.1GENCODE basic
ENST00000377735.3DMWD-0013292649aaENSP00000366964.3
 
Protein coding
G5E9A7 Q8WUW6 -GENCODE basic
ENST00000537879.1DMWD-00384364aaENSP00000444820.1
 
Protein coding
H0YGU4 -CDS 5' incomplete
ENST00000602829.1DMWD-009655161aaENSP00000473377.1
 
Protein coding
--CDS 5' incomplete
ENST00000598237.1DMWD-006643149aaENSP00000473415.1
 
Protein coding
--CDS 5' incomplete
ENST00000597053.1DMWD-007370102aaENSP00000473426.1
 
Protein coding
R4GN01 -CDS 5' incomplete
ENST00000601370.1DMWD-0051010No protein-
 
Processed transcript
---
ENST00000602469.1DMWD-008782No protein-
 
Retained intron
---
Statistics

Exons: 1, Coding exons: 0, Transcript length: 782 bps,

Version

ENST00000602469.1

Type

Retained intron

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:
OTTHUMT00000467550 (version 1)