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Human (GRCh38.p14)
Description

FSHD region gene 1 [Source:HGNC Symbol;Acc:HGNC:3954]

Gene Synonyms

FRG1A, FSG1

About this transcript

This transcript has 9 exons, is annotated with 9 domains and features, is associated with 11429 variant alleles and maps to 331 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000637998.2FRG1-230978258aaENSP00000489690.1
 
Protein coding
Q14331 -Ensembl CanonicalGENCODE PrimaryGENCODE Basic
ENST00000636021.1FRG1-224755102aaENSP00000490846.1
 
Protein coding
E9PLY7 -CDS 3' incomplete
ENST00000636883.1FRG1-227738116aaENSP00000489702.1
 
Protein coding
E9PRR7 -CDS 3' incomplete
ENST00000711575.1FRG1-231874190aaENSP00000518805.1
 
Nonsense mediated decay
A0AAA9YHY9 --
ENST00000636553.1FRG1-22571442aaENSP00000490222.1
 
Nonsense mediated decay
E9PI42 --
ENST00000636972.1FRG1-22842184aaENSP00000489820.1
 
Nonsense mediated decay
J3KSQ7 -CDS 5' incomplete
ENST00000637166.1FRG1-229838No protein-
 
Protein coding CDS not defined
---
ENST00000636688.1FRG1-226340No protein-
 
Protein coding CDS not defined
---
ENST00000711576.1FRG1-2323097No protein-
 
Retained intron
---
Statistics

Exons: 9, Coding exons: 9, Transcript length: 978 bps, Translation length: 258 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q14331

Version

ENST00000637998.2

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.