Transcript: ENSSSCT00000004032.5 THRAP3-201

Description

thyroid hormone receptor associated protein 3 [Source:VGNC Symbol;Acc:VGNC:93964]

Location

About this transcript

This transcript has 14 exons, is annotated with 34 domains and features, is associated with 947 variant alleles and maps to 38 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000031573.4	THRAP3-202	4447	958aa	ENSSSCP00000023804.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1VYM7 A0A5K1VE26	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,
ENSSSCT00000004032.5	THRAP3-201	2944	914aa	ENSSSCP00000003941.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1TMJ8 F1SV47	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: 14, Coding exons: 11, Transcript length: 2,944 bps, Translation length: 914 residues

Version

ENSSSCT00000004032.5

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.