Human (GRCh38.p14)
Description

DiGeorge syndrome critical region gene 6 like [Source:HGNC Symbol;Acc:HGNC:18551]

Gene Synonyms

FLJ10666

Location
About this transcript

This transcript has 5 exons, is annotated with 6 domains and features, is associated with 2780 variant alleles and maps to 422 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000248879.8DGCR6L-2011172220aaENSP00000248879.2
 
Protein coding
CCDS13778Q9BY27 NM_033257.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000405465.3DGCR6L-202962182aaENSP00000386052.3
 
Protein coding
B5MCQ4 -GENCODE basicTSL:3
ENST00000443409.1DGCR6L-20393597aaENSP00000403341.1
 
Nonsense mediated decay
F8WCX1 -TSL:1
Statistics

Exons: 5, Coding exons: 5, Transcript length: 1,172 bps, Translation length: 220 residues

MANE

This MANE Select transcript contains ENSP00000248879 and matches to NM_033257.4 and NP_150282.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9BY27

CCDS

This transcript is a member of the Human CCDS set: CCDS13778

Transcript Support Level (TSL)

TSL:1

Version

ENST00000248879.8

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.