Transcript: ENST00000304646.3 OR1F1-201

Description

olfactory receptor family 1 subfamily F member 1 [Source:HGNC Symbol;Acc:HGNC:8194]

Gene Synonyms

OLFMF, OR16-36, OR16-37, OR16-88, OR16-89, OR16-90, OR1F10, OR1F13P, OR1F4, OR1F5, OR1F6, OR1F7, OR1F8, OR1F9, OR3-145

Location

Chromosome 16: 3,188,204-3,206,556 forward strand.

About this transcript

This transcript has 4 exons, is annotated with 24 domains and features, is associated with 11428 variant alleles and maps to 498 oligo probes.

Gene

This transcript is a product of gene ENSG00000168124.3 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000304646.3	OR1F1-201	2748	312aa	ENSP00000305424.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS10496	O43749	NM_001370640.6	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,
ENST00000652759.1	OR1F1-203	1637	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-	-
ENST00000576468.1	OR1F1-202	629	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-	TSL 3: A transcript where the only support is from a single EST 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:3,

Summary

Statistics

Exons: 4, Coding exons: 1, Transcript length: 2,748 bps, Translation length: 312 residues

MANE

This MANE Select transcript contains ENSP00000305424 and matches to NM_001370640.6 and NP_001357569.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: O43749

CCDS

This transcript is a member of the Human CCDS set: CCDS10496

Transcript Support Level (TSL)

TSL:NA

Version

ENST00000304646.3

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Annotation Attributes

RNA-Seq supported partial [Definitions]

GENCODE basic gene

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

Transcript: ENST00000304646.3 OR1F1-201

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Transcript: ENST00000304646.3 OR1F1-201

Summary

About Us

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