Transcript: ENST00000450895.2 SMIM34-201

Description

small integral membrane protein 34 [Source:HGNC Symbol;Acc:HGNC:39601]

Gene Synonyms

SMIM34A

Location

Chromosome 21: 34,418,715-34,423,951 reverse strand.

About this transcript

This transcript has 2 exons, is annotated with 5 domains and features, is associated with 717 variant alleles and maps to 140 oligo probes.

Gene

This transcript is a product of gene ENSG00000243627.6 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000450895.2	SMIM34-201	1035	139aa	ENSP00000397039.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS93093	A8MWV9	NM_001367348.2	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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.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 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,
ENST00000850648.2	SMIM34-202	2296	139aa	ENSP00000521043.1	Nonsense mediated decay	CCDS93093	-	-	-

Summary

Statistics

Exons: 2, Coding exons: 2, Transcript length: 1,035 bps, Translation length: 139 residues

MANE

This MANE Select transcript contains ENSP00000397039 and matches to NM_001367348.2 and NP_001354277.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: A8MWV9

CCDS

This transcript is a member of the Human CCDS set: CCDS93093

Transcript Support Level (TSL)

TSL:1

Version

ENST00000450895.2

Type

Protein coding

Annotation Method

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

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

GENCODE primary gene

This transcript is a member of the Gencode Primary gene set.

Transcript: ENST00000450895.2 SMIM34-201

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Transcript: ENST00000450895.2 SMIM34-201

Summary

About Us

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