Transcript: ENST00000630865.1 NCS1-203

Description

neuronal calcium sensor 1 [Source:HGNC Symbol;Acc:HGNC:3953]

Gene Synonyms

FREQ, NCS-1

Location

Chromosome 9: 130,200,432-130,233,375 forward strand.

About this transcript

This transcript has 8 exons, is annotated with 24 domains and features, is associated with 15568 variant alleles and maps to 275 oligo probes.

Gene

This transcript is a product of gene ENSG00000107130.10 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000372398.6	NCS1-201	5164	190aa	ENSP00000361475.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS6932	P62166-1	NM_014286.4	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,
ENST00000630865.1	NCS1-203	1092	172aa	ENSP00000486695.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS78448	P62166-2	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 3: A transcript where the only support is from a single EST 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:3,
ENST00000493042.1	NCS1-202	232	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-	TSL 3: A transcript where the only support is from a single EST 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:3,

Summary

Statistics

Exons: 8, Coding exons: 7, Transcript length: 1,092 bps, Translation length: 172 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P62166

CCDS

This transcript is a member of the Human CCDS set: CCDS78448

Transcript Support Level (TSL)

TSL:3

Version

ENST00000630865.1

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

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

Transcript: ENST00000630865.1 NCS1-203

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Transcript: ENST00000630865.1 NCS1-203

Summary

About Us

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