Human (GRCh38.p14)
Description

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

Location

Chromosome 3: 49,412,212-49,416,476 forward strand.

GRCh38:CM000665.2

About this gene

This gene has 6 transcripts (splice variants) and 173 orthologues.

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