Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
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ID History
- Gene history

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Gene: NAA38 ENSPTRG00000008712

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Description

N-alpha-acetyltransferase 38, NatC auxiliary subunit [Source:VGNC Symbol;Acc:VGNC:12555]

Location

Chromosome 17: 8,144,006-8,153,822 reverse strand.

Pan_tro_3.0:CM000331.3

About this gene

This gene has 2 transcripts (splice variants) and 189 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000016049.3	NAA38-201	882	135aa	ENSPTRP00000014851.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2YC85 H2QC58	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 P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5,
ENSPTRT00000016050.3	NAA38-202	300	99aa	ENSPTRP00000014852.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2X7C3 H2QC59	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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