Gene: IGHV8-51-1 ENSG00000254167

Description

immunoglobulin heavy variable IGHV8-51-1 (non-functional) [Source:HGNC Symbol;Acc:HGNC:5704]

Gene Synonyms

IGHV(III)-51-1, IGHVIII-51-1

Location

Chromosome 14: 106,583,501-106,583,807 reverse strand.

GRCh38:CM000676.2

View alleles of this gene on alternative sequences

About this gene

This gene has 1 transcript (splice variant), 1 gene allele, 235 orthologues and 82 paralogues.

Transcripts

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Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000519403.2	IGHV8-51-1-201	307	102aa	ENSP00000503582.1	Variable chain immunoglobulin gene that undergoes somatic recombination before transcriptionIG V gene		A0A7I2V3P8	-	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 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, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

Gene: IGHV8-51-1 ENSG00000254167

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Gene: IGHV8-51-1 ENSG00000254167

Summary

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