Human (GRCh38.p14)
Description

T-box transcription factor 22 [Source:HGNC Symbol;Acc:HGNC:11600]

Gene Synonyms

CLPA, CPX

Location
About this transcript

This transcript has 9 exons, is annotated with 24 domains and features, is associated with 6516 variant alleles and maps to 287 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000373296.8TBX22-2022363520aaENSP00000362393.3
 
Protein coding
CCDS14445Q9Y458-1 NM_001109878.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000373294.8TBX22-2012249520aaENSP00000362390.5
 
Protein coding
CCDS14445Q9Y458-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000626498.2TBX22-2041955127aaENSP00000487527.1
 
Nonsense mediated decay
A0A0D9SGI2 -TSL:2
ENST00000626877.1TBX22-2052100No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000476373.1TBX22-203506No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 9, Coding exons: 8, Transcript length: 2,363 bps, Translation length: 520 residues

MANE

This MANE Select transcript contains ENSP00000362393 and matches to NM_001109878.2 and NP_001103348.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9Y458

CCDS

This transcript is a member of the Human CCDS set: CCDS14445

Transcript Support Level (TSL)

TSL:5

Version

ENST00000373296.8

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.

Annotation Attributes

RNA-Seq supported only [Definitions]

GENCODE basic gene

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