Description

RPL17-C18orf32 readthrough [Source:HGNC Symbol;Acc:HGNC:44661]

Location
INSDC coordinates

chromosome:GRCh38:CM000680.2:49481681:49491586:1

Transcripts

This gene has 3 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
RPL17-C18orf32-001ENST000005848951440228 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS58622J3KRB3 J3KSJ0 J3QS96
NM_001199355
NP_001186284
TSL:3

TSL3:The only support for this transcript is from a single EST.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
RPL17-C18orf32-003ENST00000332968928190 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS62443--TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
RPL17-C18orf32-002ENST000005779101012184 aa
 
Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins.
CCDS45865A0A024R261 J3KRB3 J3KRX5
J3KSJ0 J3QQT2 J3QS96
-TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

APPRIS PIAPPRIS principal isoform
Glossary entry for APPRIS
APPRIS website

Gene-based displays