Description

ring finger protein 39 [Source:HGNC Symbol;Acc:HGNC:18064]

Synonyms

HZFw1, LIRF

Location
INSDC coordinates

chromosome:GRCh38:CM000668.2:30070266:30075887:1

Transcripts



This gene has 2 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
RNF39-001ENST000002443602206420 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS4673Q96QB5 Q9H2S5 NM_025236
NP_079512
TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

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).APPRIS PIAPPRIS principal isoform [01-09-2014]
Glossary entry for APPRIS
APPRIS website
RNF39-002ENST000003767511970354 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS4674Q9H2S5 NM_170769
NP_739575
TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

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).

Gene-based displays