Transcript: ENST00000643046.2 CIST1-203

Description

colon, intestine and stomach enriched 1 [Source:HGNC Symbol;Acc:HGNC:55823]

Location

Chromosome 19: 18,250,034-18,255,362 reverse strand.

About this transcript

This transcript has 4 exons, is annotated with 8 domains and features, is associated with 2493 variant alleles and maps to 189 oligo probes.

Gene

This transcript is a product of gene ENSG00000284797.2 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000643046.2	CIST1-203	856	234aa	ENSP00000496487.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS92568	A0A2R8Y7Y5	NM_001396036.2	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,
ENST00000596647.1	CIST1-201	619	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,
ENST00000600667.2	CIST1-202	702	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	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: 4, Coding exons: 4, Transcript length: 856 bps, Translation length: 234 residues

MANE

This MANE Select transcript contains ENSP00000496487 and matches to NM_001396036.2 and NP_001382965.1

CCDS

This transcript is a member of the Human CCDS set: CCDS92568

Version

ENST00000643046.2

Type

Protein coding

Annotation Method

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

Annotation Attributes

RNA-Seq supported partial [Definitions]

GENCODE basic gene

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

Transcript: ENST00000643046.2 CIST1-203

Summary

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Transcript: ENST00000643046.2 CIST1-203

Summary

About Us

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