Human (GRCh37.p13)
Description

Wolfram syndrome 1 (wolframin) [Source:HGNC Symbol;Acc:12762]

Gene Synonyms

DFNA14, DFNA38, DFNA6, DIDMOAD, WFRS, WFS, WFSL

Location
About this transcript

This transcript has 5 exons, is associated with 11284 variant alleles and maps to 385 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000226760.1WFS1-0013640890aaENSP00000226760.1
 
Protein coding
CCDS3386B4DJ99 O76024 NM_006005.3GENCODE basic
ENST00000503569.1WFS1-0083255890aaENSP00000423337.1
 
Protein coding
CCDS3386B4DJ99 O76024 -GENCODE basic
ENST00000506362.1WFS1-007755252aaENSP00000424103.1
 
Protein coding
--CDS 5' and 3' incomplete
ENST00000507765.1WFS1-0043655No protein-
 
Retained intron
---
ENST00000506588.1WFS1-005587No protein-
 
Retained intron
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ENST00000513395.1WFS1-006570No protein-
 
Retained intron
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Statistics

Exons: 5, Coding exons: 0, Transcript length: 3,655 bps,

Version

ENST00000507765.1

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:
OTTHUMT00000358653 (version 1)