H4 clustered histone 14 [Source:HGNC Symbol;Acc:HGNC:4794]
H4/N, H4F2, H4FN, HIST2H4, HIST2H4A
Chromosome 1: 149,832,670-149,834,631 forward strand.
This transcript has 2 exons, is annotated with 747 domains and features, is associated with 6 variant alleles and maps to 529 oligo probes.
This transcript is a product of gene ENSG00000270882.3 Show transcript tableHide transcript table
| Transcript ID | Name | bp | Protein | Translation ID | Biotype | CCDS | UniProt Match | RefSeq Match | Flags |
|---|---|---|---|---|---|---|---|---|---|
| ENST00000578186.3 | H4C14-201 | 396 | 103aa | ENSP00000462667.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | CCDS30847 | B2R4R0 P62805 | NM_003548.2 | 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, 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, |
| ENST00000618193.1 | H4C14-204 | 1547 | 103aa | ENSP00000478786.1 | Nonsense mediated decay | CCDS30847 | B2R4R0 P62805 | - | 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, |
| ENST00000614272.1 | H4C14-203 | 942 | 103aa | ENSP00000478519.1 | Nonsense mediated decay | CCDS30847 | B2R4R0 P62805 | - | 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, |
| ENST00000613412.1 | H4C14-202 | 610 | 103aa | ENSP00000481343.1 | Nonsense mediated decay | CCDS30847 | B2R4R0 P62805 | - | 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, |