Human (GRCh38.p14)
Description

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

Gene Synonyms

MSH5-C6ORF26

Location

Scaffold HSCHR6_MHC_DBB_CTG1: 2,987,786-3,012,625 forward strand.

GRCh38:GL000252.2

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
ENST00000583103.5MSH5-SAPCD1-2203992851aaENSP00000462078.1
 
Nonsense mediated decay
A0A024RCV8 -Ensembl CanonicalGENCODE basicTSL:1
ENST00000476578.5MSH5-SAPCD1-2182217264aaENSP00000463749.1
 
Nonsense mediated decay
H0YF11 -TSL:1CDS 5' incomplete
ENST00000496211.1MSH5-SAPCD1-21995029aaENSP00000463412.1
 
Nonsense mediated decay
H0YEB2 -TSL:2CDS 5' incomplete
ENST00000469909.2MSH5-SAPCD1-217711No protein-
 
Protein coding CDS not defined
--TSL:3