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 18719 variant alleles and maps to 301 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: 1,362 bps, Translation length: 200 residues

MANE

This MANE Select transcript contains ENSP00000278980 and matches to NM_053041.3 and NP_444269.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q86VX2

CCDS

This transcript is a member of the Human CCDS set: CCDS42864

Transcript Support Level (TSL)

TSL:1

Version

ENST00000278980.11

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.