Human (GRCh38.p14)
Description

jumping translocation breakpoint [Source:HGNC Symbol;Acc:HGNC:6201]

Gene Synonyms

HJT, PAR

About this transcript

This transcript has 5 exons, is annotated with 7 domains and features, is associated with 1722 variant alleles and maps to 677 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000271843.9JTB-2011273146aaENSP00000271843.4
 
Protein coding
CCDS1057O76095-1 NM_006694.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000368589.5JTB-2031216117aaENSP00000357578.1
 
Protein coding
O76095-2 -GENCODE basicTSL:2
ENST00000356648.5JTB-2021040117aaENSP00000349069.1
 
Protein coding
O76095-2 -GENCODE basicTSL:2
ENST00000428469.1JTB-204520117aaENSP00000395250.1
 
Protein coding
O76095-2 -TSL:3CDS 3' incomplete
ENST00000471173.1JTB-206754No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000461365.1JTB-205542No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 5, Coding exons: 5, Transcript length: 1,273 bps, Translation length: 146 residues

MANE

This MANE Select transcript contains ENSP00000271843 and matches to NM_006694.4 and NP_006685.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: O76095

CCDS

This transcript is a member of the Human CCDS set: CCDS1057

Transcript Support Level (TSL)

TSL:1

Version

ENST00000271843.9

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.