Human (GRCh38.p14)
Description

CHKB-CPT1B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41998]

Location
About this transcript

This transcript has 23 exons, is annotated with 1 domain and feature, is associated with 5741 variant alleles and maps to 1062 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000453634.5CHKB-CPT1B-202281660aaENSP00000457031.1
 
Nonsense mediated decay
H3BT56 -Ensembl CanonicalGENCODE basicAPPRIS P1TSL:5CDS 5' incomplete
ENST00000452668.1CHKB-CPT1B-201546No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000492556.5CHKB-CPT1B-2034906No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 23, Coding exons: 3, Transcript length: 2,816 bps, Translation length: 60 residues

Transcript Support Level (TSL)

TSL:5

Incomplete CDS

CDS 5' incomplete

Version

ENST00000453634.5

Type

Nonsense mediated decay

Annotation Method

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

GENCODE basic gene

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