Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
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Gene: HAUS6 ENSBTAG00000019843

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Description

HAUS augmin like complex subunit 6 [Source:VGNC Symbol;Acc:VGNC:29761]

Location

Primary_assembly 8: 25,138,098-25,180,190 forward strand.

ARS-UCD1.3:CM008175.2

About this gene

This gene has 2 transcripts (splice variants) and 202 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000031479.6	HAUS6-202	3939	912aa	ENSBTAP00000031434.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BG87	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,
ENSBTAT00000114956.1	HAUS6-201	3900	899aa	ENSBTAP00000092058.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,

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Summary

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