Human (GRCh38.p14)
Description

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

Gene Synonyms

FRG1A, FSG1

Location

Scaffold HSCHR4_6_CTG12: 278,318-300,735 forward strand.

GRCh38:KI270896.1

View this gene on the primary assembly.

About this gene

This gene has 7 transcripts (splice variants), 1 gene allele and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000620886.3FRG1-2101074258aaENSP00000483471.1
 
Protein coding
Q14331 -Ensembl CanonicalGENCODE basicTSL:1
ENST00000624356.3FRG1-211755102aaENSP00000485342.2
 
Protein coding
E9PLY7 -TSL:5CDS 3' incomplete
ENST00000627466.2FRG1-214738116aaENSP00000486212.1
 
Protein coding
E9PRR7 -TSL:5CDS 3' incomplete
ENST00000625559.2FRG1-21271442aaENSP00000486096.1
 
Nonsense mediated decay
E9PI42 -TSL:5
ENST00000627980.1FRG1-21542184aaENSP00000487528.1
 
Nonsense mediated decay
J3KSQ7 -TSL:3CDS 5' incomplete
ENST00000629010.1FRG1-216838No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000626875.1FRG1-213340No protein-
 
Protein coding CDS not defined
--TSL:2