Description

heterogeneous nuclear ribonucleoprotein C-like 1 [Source:HGNC Symbol;Acc:HGNC:29295]

Synonyms

HNRPCL1

Location
INSDC coordinates

chromosome:GRCh38:CM000663.2:12847377:12947578:1

About this gene

This gene has 2 transcripts (splice variants), 84 orthologues, 6 paralogues, is a member of 1 Ensembl protein family and is associated with 164 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
HNRNPCL1-201ENST000006170441156293aaENSP00000479365
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS30591O60812 -TSL:1

Transcript Support Level 1, when transcripts 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 P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

HNRNPCL1-001ENST000003178691108293aaENSP00000365370
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS30591O60812 NM_001013631
NP_001013653
TSL:1

Transcript Support Level 1, when transcripts 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 P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Gene-based displays