Human (GRCh38.p14)
Description

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

Gene Synonyms

FLJ00007

About this transcript

This transcript has 20 exons, is annotated with 35 domains and features, is associated with 6058 variant alleles and maps to 687 oligo probes.

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
Statistics

Exons: 20, Coding exons: 20, Transcript length: 4,319 bps, Translation length: 690 residues

MANE

This MANE Select transcript contains ENSP00000399259 and matches to NM_033449.3 and NP_258260.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q86WN1

CCDS

This transcript is a member of the Human CCDS set: CCDS47295

Transcript Support Level (TSL)

TSL:1

Version

ENST00000435817.7

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.