Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
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Comparative Genomics
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Gene: CHAF1B ENSBTAG00000011880

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Description

chromatin assembly factor 1 subunit B [Source:VGNC Symbol;Acc:VGNC:27267]

Location

Primary_assembly 1: 148,658,317-148,683,915 forward strand.

ARS-UCD1.3:CM008168.2

About this gene

This gene has 2 transcripts (splice variants) and 208 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000015764.6	CHAF1B-201	2257	575aa	ENSBTAP00000015764.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A5D9H4	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,
ENSBTAT00000082170.2	CHAF1B-202	2062	510aa	ENSBTAP00000058552.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A5D9H4	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,

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Summary

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