Transcript: ENSGALT00010058031.1 GALNT6-202

Description

polypeptide N-acetylgalactosaminyltransferase 6 [Source:NCBI gene (formerly Entrezgene);Acc:429501]

Location

About this transcript

This transcript has 12 exons, is annotated with 21 domains and features, is associated with 703 variant alleles and maps to 24 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010058031.1	GALNT6-202	3015	665aa	ENSGALP00010035209.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0ZY16	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,
ENSGALT00010058037.1	GALNT6-201	3310	610aa	ENSGALP00010035215.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0ZWH1	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: 12, Coding exons: 11, Transcript length: 3,015 bps, Translation length: 665 residues

Version

ENSGALT00010058031.1

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.