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

Chromosome 22: 23,765,834-23,767,972 reverse strand.

GRCh38:CM000684.2

View alleles of this gene on alternative sequences

About this gene

This gene has 5 transcripts (splice variants), 1 gene allele, 161 orthologues, 1 paralogue and is associated with 7 phenotypes.

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