Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: HIST1H4A ENSG00000278637

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Description

histone cluster 1 H4 family member a [Source:HGNC Symbol;Acc:HGNC:4781]

Synonyms

H4FA

Location

Chromosome 6: 26,021,679-26,021,990 forward strand.

GRCh38:CM000668.2

About this gene

This gene has 1 transcript (splice variant), 33 orthologues, 14 paralogues, is a member of 1 Ensembl protein family and is associated with 1 phenotype.

Transcripts

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Name	Transcript ID	bp	Protein	Translation ID	Biotype	CCDS	UniProt	RefSeq	Flags
HIST1H4A-201	ENST00000617569.1	312	103aa	ENSP00000479106	<p>Genes and/or transcript that contains an open reading frame (ORF).</p>Protein coding	CCDS4571	B2R4R0 P62805	NM_003538 NP_003529	<p>Transcript Support Level Not Analysed. Pseudogenes, single exon transcripts, HLA, T-cell receptor and Ig transcripts are not analysed and therefore not given any of the TSL categories.</p><p>The <a href="https://genome.ucsc.edu/cgi-bin/hgc?hgsid=423831555_sqRhAapgi8atmzzBPBAz8Me5797J&c=chr14&o=94517268&t=94547548&g=wgEncodeGencodeCompV19&i=ENST00000544005.1#tsl" target="_self">Transcript Support Level</a> (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.</p>TSL:NAThe GENCODE set is the gene set for human and mouse. <a href="/Help/Glossary?id=500" class="popup">GENCODE Basic</a> is a subset of representative transcripts (splice variants).GENCODE basic<p>PRINCIPAL1 - APPRIS candidate principal isoform.</p><p><a class="popup" href="/Homo_sapiens/Help/Glossary?id=521">APPRIS</a> is a system to annotate alternatively spliced transcripts based on a range of computational methods.</p>APPRIS P1

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Summary

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Gene-based displays