Human (GRCh38.p14)
Description

HSPB2-C11orf52 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41996]

About this transcript

This transcript has 3 exons, is associated with 2679 variant alleles and maps to 326 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000527616.1HSPB2-C11orf52-201892182aaENSP00000457706.1
 
Nonsense mediated decay
CCDS8352A8KAH6 -Ensembl CanonicalGENCODE basicAPPRIS P5TSL:2
ENST00000534100.1HSPB2-C11orf52-202152152aaENSP00000455839.1
 
Nonsense mediated decay
E9PN16 -APPRIS ALT2TSL:2
Statistics

Exons: 3, Coding exons: 2, Transcript length: 892 bps, Translation length: 182 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS8352

Transcript Support Level (TSL)

TSL:2

Version

ENST00000527616.1

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.