Human (GRCh38.p14)
Description

coiled-coil-helix-coiled-coil-helix domain containing 10 [Source:HGNC Symbol;Acc:HGNC:15559]

Gene Synonyms

C22ORF16, MIX17A, N27C7-4

Location
About this transcript

This transcript has 4 exons, is annotated with 11 domains and features, is associated with 1342 variant alleles and maps to 224 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000484558.3CHCHD10-202700142aaENSP00000418428.3
 
Protein coding
CCDS13815Q8WYQ3 NM_213720.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000401675.7CHCHD10-201691149aaENSP00000384973.3
 
Protein coding
CCDS77659B5MBW9 -GENCODE basicTSL:5
ENST00000520222.1CHCHD10-20438455aaENSP00000430042.1
 
Protein coding
E5RH03 -GENCODE basicTSL:3
ENST00000517886.1CHCHD10-20349499aaENSP00000429976.1
 
Nonsense mediated decay
E5RGN4 -TSL:3
ENST00000523865.1CHCHD10-205490No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 4, Coding exons: 4, Transcript length: 700 bps, Translation length: 142 residues

MANE

This MANE Select transcript contains ENSP00000418428 and matches to NM_213720.3 and NP_998885.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8WYQ3

CCDS

This transcript is a member of the Human CCDS set: CCDS13815

Transcript Support Level (TSL)

TSL:1

Version

ENST00000484558.3

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.