Transcript: ENSRNOT00000066791.4 Gtf2h1-201

Description

general transcription factor IIH subunit 1 [Source:RGD Symbol;Acc:1308225]

Gene Synonyms

LOC361580

Location

About this transcript

This transcript has 16 exons, is annotated with 17 domains and features, is associated with 72 variant alleles and maps to 239 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000066791.4	Gtf2h1-201	2232	569aa	ENSRNOP00000063357.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZYG3	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 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,
ENSRNOT00000087920.3	Gtf2h1-202	3011	547aa	ENSRNOP00000069965.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JWQ0	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,

Summary

Statistics

Exons: 16, Coding exons: 15, Transcript length: 2,232 bps, Translation length: 569 residues

Version

ENSRNOT00000066791.4

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.