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- Splice variants
- Transcript comparison
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Gene: Gm15104 ENSMUSG00000087360

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Description

predicted gene 15104 [Source:MGI Symbol;Acc:MGI:3705199]

Location

Chromosome X: 149,088,432-149,119,355 reverse strand.

GRCm39:CM001013.3

About this gene

This gene has 8 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	Flags
ENSMUST00000313501.1	Gm15104-203	871	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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary,
ENSMUST00000313505.1	Gm15104-207	1666	No protein	-	lncRNA		A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENSMUST00000313503.1	Gm15104-205	1571	No protein	-	lncRNA		-
ENSMUST00000132626.3	Gm15104-201	1452	No protein	-	lncRNA		TSL 1: A transcript where all splice junctions 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, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000165760.3	Gm15104-202	1417	No protein	-	lncRNA		TSL NA: A transcript that was not analysed for TSL. 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:NA,
ENSMUST00000313502.1	Gm15104-204	1389	No protein	-	lncRNA		-
ENSMUST00000313504.1	Gm15104-206	1360	No protein	-	lncRNA		-
ENSMUST00000313506.1	Gm15104-208	964	No protein	-	lncRNA		-

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Summary

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