Transcript: ENSBTAT00000026784.4 DNASE1-202

Description

deoxyribonuclease 1 [Source:VGNC Symbol;Acc:VGNC:28132]

Location

About this transcript

This transcript has 8 exons, is annotated with 20 domains and features and is associated with 1091 variant alleles.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000102429.1	DNASE1-201	1782	421aa	ENSBTAP00000099781.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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, 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,
ENSBTAT00000026784.4	DNASE1-202	1562	290aa	ENSBTAP00000026784.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P00639	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: 8, Coding exons: 7, Transcript length: 1,562 bps, Translation length: 290 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P00639

Version

ENSBTAT00000026784.4

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.