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

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Gene: asap1a ENSDARG00000029463

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Description

ArfGAP with SH3 domain, ankyrin repeat and PH domain 1a [Source:NCBI gene (formerly Entrezgene);Acc:100170829]

Location

Chromosome 2: 32,263,215-32,356,539 reverse strand.

GRCz11:CM002886.2

About this gene

This gene has 3 transcripts (splice variants), 163 orthologues and 34 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000144870.3	asap1a-202	3615	1132aa	ENSDARP00000120481.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000169316.2	asap1a-203	8880	1097aa	ENSDARP00000136448.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4IM47	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,
ENSDART00000077151.4	asap1a-201	3421	1077aa	ENSDARP00000071619.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B3DI91	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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