Human (GRCh38.p14)
Description

T cell leukemia translocation altered [Source:HGNC Symbol;Acc:HGNC:11692]

Location
About this transcript

This transcript has 2 exons, is associated with 422 variant alleles and maps to 244 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000273590.4TCTA-2011930103aaENSP00000273590.3
 
Protein coding
CCDS2796P57738 NM_022171.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000493381.1TCTA-2051081No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000487432.1TCTA-203892No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000488385.1TCTA-204800No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000482193.1TCTA-202590No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000497786.1TCTA-206587No protein-
 
Protein coding CDS not defined
--TSL:4
Statistics

Exons: 2, Coding exons: 0, Transcript length: 587 bps,

Transcript Support Level (TSL)

TSL:4

Version

ENST00000497786.1

Type

Protein coding CDS not defined

Annotation Method

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