Transcript: ENST00000424805.1 PNMA3-201

Description

PNMA family member 3 [Source:HGNC Symbol;Acc:HGNC:18742]

Gene Synonyms

MA3, MA5, MGC132756, MGC132758

Location

Chromosome X: 153,056,482-153,060,462 forward strand.

About this transcript

This transcript has 3 exons, is annotated with 1 domain and feature, is associated with 1783 variant alleles and maps to 283 oligo probes.

Gene

This transcript is a product of gene ENSG00000183837.10 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000593810.3	PNMA3-202	3682	463aa	ENSP00000469445.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS35435	Q9UL41-1	NM_013364.6	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, 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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1, TSL NA: A transcript that was not analysed for TSL. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:NA,
ENST00000619635.1	PNMA3-203	3627	455aa	ENSP00000480719.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS65344	Q9UL41-2	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENST00000424805.1	PNMA3-201	3158	463aa	ENSP00000390576.1	Nonsense mediated decay	CCDS35435	Q9UL41-1	-	TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5,

Summary

Statistics

Exons: 3, Coding exons: 1, Transcript length: 3,158 bps, Translation length: 463 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UL41

CCDS

This transcript is a member of the Human CCDS set: CCDS35435

Transcript Support Level (TSL)

TSL:5

Version

ENST00000424805.1

Type

Nonsense mediated decay

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Transcript: ENST00000424805.1 PNMA3-201

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Transcript: ENST00000424805.1 PNMA3-201

Summary

About Us

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