Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: MYH14 ENSPTRG00000011333

.

Description

myosin heavy chain 14 [Source:VGNC Symbol;Acc:VGNC:13233]

Location

Chromosome 19: 52,378,439-52,485,254 forward strand.

Pan_tro_3.0:CM000333.3

About this gene

This gene has 5 transcripts (splice variants), 194 orthologues and 46 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000101557.1	MYH14-203	7195	2036aa	ENSPTRP00000065124.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RKA2 A0A6D2VVH5	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, APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as the principal variant. 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 P5,
ENSPTRT00000049528.4	MYH14-201	6822	2003aa	ENSPTRP00000048538.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8J167 A0A6D2X2J8	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSPTRT00000093871.1	MYH14-202	6798	1995aa	ENSPTRP00000076311.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8J168 A0A6D2WBN4	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSPTRT00000086985.1	MYH14-205	6154	638aa	ENSPTRP00000085608.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3T8U0 A0A6D2X9A3	-
ENSPTRT00000094160.1	MYH14-204	6018	2005aa	ENSPTRP00000089063.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TIK8	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

.

Summary

.

.