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 29 exons, is annotated with 1 domain and feature, is associated with 10879 variant alleles and maps to 4763 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000493662.6MSH5-SAPCD1-2073991851aaENSP00000417871.2
 
Nonsense mediated decay
A0A024RCV4 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: 29, Coding exons: 24, Transcript length: 3,991 bps, Translation length: 851 residues

Transcript Support Level (TSL)

TSL:1

Version

ENST00000493662.6

Type

Nonsense mediated decay

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.