Human (GRCh38.p14)
Description

COMM domain containing 7 [Source:HGNC Symbol;Acc:HGNC:16223]

Gene Synonyms

C20ORF92, DJ1085F17.3

Location
About this transcript

This transcript has 9 exons, is annotated with 5 domains and features, is associated with 18707 variant alleles and maps to 271 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000278980.11COMMD7-2011362200aaENSP00000278980.6
 
Protein coding
CCDS42864Q86VX2-1 NM_053041.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:1
ENST00000446419.6COMMD7-2021343199aaENSP00000395339.1
 
Protein coding
CCDS46587Q86VX2-2 -GENCODE basicAPPRIS ALT1TSL:2
ENST00000474815.2COMMD7-203488157aaENSP00000476443.1
 
Protein coding
V9GY66 -TSL:5CDS 3' incomplete
ENST00000610160.1COMMD7-204198757aaENSP00000476617.1
 
Nonsense mediated decay
V9GYC5 -TSL:2
Statistics

Exons: 9, Coding exons: 9, Transcript length: 1,343 bps, Translation length: 199 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q86VX2

CCDS

This transcript is a member of the Human CCDS set: CCDS46587

Transcript Support Level (TSL)

TSL:2

Version

ENST00000446419.6

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.