Description

claudin 19 [Source:HGNC Symbol;Acc:HGNC:2040]

Location
INSDC coordinates

chromosome:GRCh38:CM000663.2:42733093:42740254:1

Transcripts

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

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
CLDN19-201ENST000005397493517218 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS53306Q8N6F1 NM_001185117
NP_001172046
TSL:2

TSL2: The best supporting mRNA is flagged as suspect or the support is from multiple ESTs.

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).
CLDN19-001ENST000002963872859224 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS471Q8N6F1 NM_148960
NP_683763
TSL:2

TSL2: The best supporting mRNA is flagged as suspect or the support is from multiple ESTs.

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).
CLDN19-002ENST000003725391586211 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS44125Q8N6F1 NM_001123395
NP_001116867
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
Glossary entry for APPRIS
APPRIS website

Gene-based displays