Human (GRCh38.p14)
Description

F-box and WD repeat domain containing 10 [Source:HGNC Symbol;Acc:HGNC:1211]

Gene Synonyms

C17ORF1, C17ORF1A, FBW10, HREP, SM2SH2

Location
About this transcript

This transcript has 13 exons, is annotated with 28 domains and features, is associated with 15268 variant alleles and maps to 673 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000395665.9FBXW10-20334011052aaENSP00000379025.4
 
Protein coding
CCDS11199Q5XX13-1 NM_001267585.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000308799.8FBXW10-20234561061aaENSP00000310382.4
 
Protein coding
CCDS92270Q5XX13-2 -GENCODE basicAPPRIS ALT2TSL:2
ENST00000301938.4FBXW10-2013221999aaENSP00000306937.4
 
Protein coding
CCDS58524Q5XX13-3 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000574478.1FBXW10-2053418196aaENSP00000463552.1
 
Nonsense mediated decay
J3QLH9 -TSL:1
ENST00000573605.1FBXW10-204571No protein-
 
Protein coding CDS not defined
--TSL:4
Statistics

Exons: 13, Coding exons: 13, Transcript length: 3,221 bps, Translation length: 999 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q5XX13

CCDS

This transcript is a member of the Human CCDS set: CCDS58524

Transcript Support Level (TSL)

TSL:1

Version

ENST00000301938.4

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.