Transcript: ENST00000684090.1 LHFPL3-204

Description

LHFPL tetraspan subfamily member 3 [Source:HGNC Symbol;Acc:HGNC:6589]

Gene Synonyms

LHFPL4

Location

Chromosome 7: 104,723,372-104,908,505 forward strand.

About this transcript

This transcript has 3 exons, is associated with 80651 variant alleles and maps to 200 oligo probes.

Gene

This transcript is a product of gene ENSG00000187416.13 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000424859.7	LHFPL3-202	3234	236aa	ENSP00000393128.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS94168	Q86UP9	NM_199000.3	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 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,
ENST00000401970.3	LHFPL3-201	1475	232aa	ENSP00000385374.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS94167	A1L384	-	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,
ENST00000683240.1	LHFPL3-203	2991	127aa	ENSP00000508253.1	Nonsense mediated decay		A0A804HL93	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENST00000684090.1	LHFPL3-204	2579	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-	-

Summary

Statistics

Exons: 3, Coding exons: 0, Transcript length: 2,579 bps,

Version

ENST00000684090.1

Type

Protein coding CDS not defined

Annotation Method

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

Annotation Attributes

inferred transcript model [Definitions]

RNA-Seq supported only

Transcript: ENST00000684090.1 LHFPL3-204

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Transcript: ENST00000684090.1 LHFPL3-204

Summary

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