Human (GRCh38.p14)
Description

chromobox 7 [Source:HGNC Symbol;Acc:HGNC:1557]

Location

Chromosome 22: 39,120,167-39,152,680 reverse strand.

GRCh38:CM000684.2

About this gene

This gene has 7 transcripts (splice variants), 267 orthologues and 8 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000216133.10CBX7-2014111251aaENSP00000216133.5
 
Protein coding
CCDS13986A0A024R1Q2 O95931 NM_175709.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000401405.7CBX7-202784158aaENSP00000384035.3
 
Protein coding
CCDS87028B0QYP2 -GENCODE basicTSL:1
ENST00000434260.1CBX7-203472121aaENSP00000410896.1
 
Protein coding
B0QYP3 -TSL:3CDS 3' incomplete
ENST00000475962.5CBX7-204451No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000482294.1CBX7-2063014No protein-
 
Retained intron
--TSL:2
ENST00000490741.1CBX7-207734No protein-
 
Retained intron
--TSL:3
ENST00000477827.1CBX7-205526No protein-
 
Retained intron
--TSL:5