Transcript: ENST00000674256.1 PRSS41-202

Description

serine protease 41 [Source:HGNC Symbol;Acc:HGNC:30715]

Gene Synonyms

TESSP1

Location

Chromosome 16: 2,798,470-2,805,304 forward strand.

About this transcript

This transcript has 5 exons, is annotated with 18 domains and features, is associated with 3985 variant alleles and maps to 193 oligo probes.

Gene

This transcript is a product of gene ENSG00000215148.11 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000399677.5	PRSS41-201	1105	305aa	ENSP00000492058.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS92090	A0A6Q8NYF4	NM_001395501.1	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2, 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,
ENST00000674256.1	PRSS41-202	1192	334aa	ENSP00000501492.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS92091	A0A6I8PU99	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

Summary

Statistics

Exons: 5, Coding exons: 5, Transcript length: 1,192 bps, Translation length: 334 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS92091

Version

ENST00000674256.1

Type

Protein coding

Annotation Method

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

Annotation Attributes

RNA-Seq supported only [Definitions]

GENCODE basic gene

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

Transcript: ENST00000674256.1 PRSS41-202

Summary

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Transcript: ENST00000674256.1 PRSS41-202

Summary

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