Transcript: ENSSSCT00000010335.4 FAM216B-201

Description

family with sequence similarity 216 member B [Source:VGNC Symbol;Acc:VGNC:87955]

Location

About this transcript

This transcript has 5 exons, is annotated with 5 domains and features, is associated with 624 variant alleles and maps to 12 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000010335.4	FAM216B-201	2040	185aa	ENSSSCP00000010067.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1LME1 F1RJX2	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,
ENSSSCT00000064788.2	FAM216B-202	1985	165aa	ENSSSCP00000057867.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BMM3 A0A8D0ZJD7	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: 2,040 bps, Translation length: 185 residues

Version

ENSSSCT00000010335.4

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.