Human (GRCh38.p14)
Description

MSH5-SAPCD1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41994]

Gene Synonyms

MSH5-C6ORF26

Location
About this transcript

This transcript has 14 exons, is associated with 2393 variant alleles and maps to 2143 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000493662.6MSH5-SAPCD1-2073991851aaENSP00000417871.2
 
Nonsense mediated decay
A0A024RCV8 -Ensembl CanonicalGENCODE basicAPPRIS P5TSL:1
ENST00000498473.6MSH5-SAPCD1-2082216264aaENSP00000419220.2
 
Nonsense mediated decay
H0YF11 -APPRIS ALT2TSL:1CDS 5' incomplete
ENST00000476085.1MSH5-SAPCD1-20595029aaENSP00000435414.1
 
Nonsense mediated decay
H0YEB2 -APPRIS ALT2TSL:2CDS 5' incomplete
ENST00000491552.1MSH5-SAPCD1-206706No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 14, Coding exons: 7, Transcript length: 2,216 bps, Translation length: 264 residues

Transcript Support Level (TSL)

TSL:1

Incomplete CDS

CDS 5' incomplete

Version

ENST00000498473.6

Type

Nonsense mediated decay

Annotation Method

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