Human (GRCh38.p14)
Description

FCH and double SH3 domains 1 [Source:HGNC Symbol;Acc:HGNC:25463]

Gene Synonyms

FLJ00007

Location

Chromosome 5: 141,639,302-141,651,418 reverse strand.

GRCh38:CM000667.2

About this gene

This gene has 10 transcripts (splice variants), 228 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000435817.7FCHSD1-2014319690aaENSP00000399259.2
 
Protein coding
CCDS47295Q86WN1-1 NM_033449.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000522783.5FCHSD1-2092477598aaENSP00000428677.1
 
Protein coding
E5RGT6 -GENCODE basicTSL:5
ENST00000519800.1FCHSD1-204802255aaENSP00000428776.1
 
Protein coding
E5RGB1 -GENCODE basicTSL:2
ENST00000518499.1FCHSD1-203714211aaENSP00000430448.1
 
Protein coding
E5RK49 -TSL:3CDS 3' incomplete
ENST00000522126.5FCHSD1-2062577409aaENSP00000427796.1
 
Nonsense mediated decay
Q86WN1-3 -TSL:2
ENST00000523856.5FCHSD1-2103932No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000518160.1FCHSD1-202719No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000522386.1FCHSD1-207581No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000522763.5FCHSD1-208443No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000520747.1FCHSD1-2053181No protein-
 
Retained intron
--TSL:2