Advanced notice of Ensembl Tools maintenance
Please note that due to planned maintenance, Ensembl Tools will be unavailable from Tuesday, September 9, at 08:30 AM BST until Wednesday, September 10, at 08:30 AM BST.
Jobs submitted during the maintenance window will be queued and processed once maintenance is complete. We apologise for the inconvenience.

Human (GRCh38.p14)
Description

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

Gene Synonyms

MSH5-C6ORF26

Location

Scaffold HSCHR6_MHC_COX_CTG1: 3,217,300-3,242,109 forward strand.

GRCh38:GL000251.2

View this gene on the primary assembly.

About this gene

This gene has 4 transcripts (splice variants) and 1 gene allele.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000480850.5MSH5-SAPCD1-2043993851aaENSP00000457803.1
 
Nonsense mediated decay
A0A024RCV8 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000469011.5MSH5-SAPCD1-2012218264aaENSP00000457337.1
 
Nonsense mediated decay
H0YF11 -TSL:1CDS 5' incomplete
ENST00000477722.1MSH5-SAPCD1-20295129aaENSP00000464606.1
 
Nonsense mediated decay
H0YEB2 -TSL:2CDS 5' incomplete
ENST00000480223.1MSH5-SAPCD1-203706No protein-
 
Protein coding CDS not defined
--TSL:3