Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: ENSG00000267215

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Description

novel transcript

Location

Chromosome 18: 59,081,911-59,085,920 forward strand.

GRCh38:CM000680.2

About this gene

This gene has 12 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	RefSeq Match	Flags
ENST00000670499.1	-	1834	No protein	-	lncRNA		-	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,
ENST00000666703.1	-	2006	No protein	-	lncRNA		-	-
ENST00000658546.1	-	1937	No protein	-	lncRNA		-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000591900.2	-	1878	No protein	-	lncRNA		-	TSL 4: A transcript where the best supporting EST is flagged as suspect The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:4,
ENST00000655415.1	-	1829	No protein	-	lncRNA		-	-
ENST00000655428.1	-	1761	No protein	-	lncRNA		-	-
ENST00000669170.1	-	1746	No protein	-	lncRNA		-	-
ENST00000663146.1	-	1613	No protein	-	lncRNA		-	-
ENST00000589729.2	-	1605	No protein	-	lncRNA		-	TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5,
ENST00000666207.1	-	1604	No protein	-	lncRNA		-	-
ENST00000656626.1	-	1597	No protein	-	lncRNA		-	-
ENST00000671255.1	-	1480	No protein	-	lncRNA		-	-

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Summary

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