Human (GRCh38.p14)
Description

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

Gene Synonyms

FRG1A, FSG1

Location

Scaffold HG2023_PATCH: 33,800-56,132 forward strand.

GRCh38:KQ983257.1

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
ENST00000636590.2FRG1-220978258aaENSP00000490541.1
 
Protein coding
Q14331 -Ensembl CanonicalGENCODE basic
ENST00000637139.1FRG1-222755102aaENSP00000489664.1
 
Protein coding
--CDS 3' incomplete
ENST00000636262.1FRG1-218738116aaENSP00000490915.1
 
Protein coding
--CDS 3' incomplete
ENST00000637604.1FRG1-22371442aaENSP00000489960.1
 
Nonsense mediated decay
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ENST00000636832.1FRG1-22142184aaENSP00000489984.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000636156.1FRG1-217838No protein-
 
Protein coding CDS not defined
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ENST00000636338.1FRG1-219340No protein-
 
Protein coding CDS not defined
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