Transcript: ENST00000396192.7 CSE1L-202

Description

chromosome segregation 1 like [Source:HGNC Symbol;Acc:HGNC:2431]

Gene Synonyms

CAS, CSE1, XPO2

Location

Chromosome 20: 49,046,246-49,096,960 forward strand.

About this transcript

This transcript has 24 exons, is annotated with 13 domains and features, is associated with 24559 variant alleles and maps to 883 oligo probes.

Gene

This transcript is a product of gene ENSG00000124207.17 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000262982.3	CSE1L-201	3550	971aa	ENSP00000262982.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS13412	P55060-1	NM_001316.4	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, 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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1, 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,
ENST00000396192.7	CSE1L-202	3459	915aa	ENSP00000379495.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS58773	P55060-4	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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,
ENST00000469700.1	CSE1L-203	1401	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-	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,

Summary

Statistics

Exons: 24, Coding exons: 23, Transcript length: 3,459 bps, Translation length: 915 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P55060

CCDS

This transcript is a member of the Human CCDS set: CCDS58773

Transcript Support Level (TSL)

TSL:5

Version

ENST00000396192.7

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

Transcript: ENST00000396192.7 CSE1L-202

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Transcript: ENST00000396192.7 CSE1L-202

Summary

About Us

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