Transcript: ENST00000696132.1 CXCL8-205

Description

C-X-C motif chemokine ligand 8 [Source:HGNC Symbol;Acc:HGNC:6025]

Gene Synonyms

3-10C, AMCF-I, B-ENAP, GCP-1, GCP1, IL-8, IL8, K60, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1, SCYB8, TSG-1

Location

Chromosome 4: 73,740,549-73,743,715 forward strand.

About this transcript

This transcript has 4 exons, is associated with 1558 variant alleles and maps to 469 oligo probes.

Gene

This transcript is a product of gene ENSG00000169429.12 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000307407.8	CXCL8-201	1642	99aa	ENSP00000306512.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS34005	A0A024RDA5 P10145	NM_000584.4	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,
ENST00000401931.1	CXCL8-202	700	95aa	ENSP00000385908.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS87231	C9J4T6	-	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,
ENST00000696131.1	CXCL8-204	2018	40aa	ENSP00000512424.1	Nonsense mediated decay		A0A8Q3SIG6	-	-
ENST00000696132.1	CXCL8-205	1742	40aa	ENSP00000512425.1	Nonsense mediated decay		A0A8Q3SIG6	-	-
ENST00000483500.1	CXCL8-203	599	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	TSL 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs 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:2,

Summary

Statistics

Exons: 4, Coding exons: 1, Transcript length: 1,742 bps, Translation length: 40 residues

Version

ENST00000696132.1

Type

Nonsense mediated decay

Annotation Method

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

Annotation Attributes

RNA-Seq supported only [Definitions]

Transcript: ENST00000696132.1 CXCL8-205

Summary

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Transcript: ENST00000696132.1 CXCL8-205

Summary

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