Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: HNRNPA3 ENSBTAG00000021580

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Description

heteroous nuclear ribonucleoprotein A3 [Source:VGNC Symbol;Acc:VGNC:50100]

Location

Primary_assembly 2: 19,658,412-19,663,871 reverse strand.

ARS-UCD2.0:CM008169.2

About this gene

This gene has 5 transcripts (splice variants), 138 orthologues and 47 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000028757.7	HNRNPA3-201	1208	396aa	ENSBTAP00000028757.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BEG2	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,
ENSBTAT00000110783.1	HNRNPA3-203	1450	380aa	ENSBTAP00000103868.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TZ00	-
ENSBTAT00000100279.1	HNRNPA3-204	1360	350aa	ENSBTAP00000085588.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SHA4	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,
ENSBTAT00000133074.1	HNRNPA3-205	1360	350aa	ENSBTAP00000081726.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SCZ0	-
ENSBTAT00000106031.1	HNRNPA3-202	1212	331aa	ENSBTAP00000087856.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SV55	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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