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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

Scaffold HSCHR22_1_CTG7: 2,196-4,805 reverse strand.

GRCh38:KI270879.1

View this gene on the primary assembly.

About this gene

This gene has 5 transcripts (splice variants), 1 gene allele and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000620558.3CHCHD10-212691149aaENSP00000480602.2
 
Protein coding
B5MBW9 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:5
ENST00000629095.1CHCHD10-2151171142aaENSP00000487006.1
 
Protein coding
Q8WYQ3 -GENCODE BasicTSL:1
ENST00000631145.1CHCHD10-21638455aaENSP00000486207.1
 
Protein coding
E5RH03 -GENCODE BasicTSL:3
ENST00000626041.1CHCHD10-21349499aaENSP00000486793.1
 
Nonsense mediated decay
E5RGN4 -TSL:3
ENST00000626885.1CHCHD10-214490No protein-
 
Retained intron
--TSL:2