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

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Gene: CHM ENSGALG00010018244

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Description

CHM, Rab escort protein 1 [Source:NCBI gene (formerly Entrezgene);Acc:422266]

Gene Synonyms

CHML

Location

Primary_assembly 4: 8,515,582-8,595,687 forward strand.

bGalGal1.mat.broiler.GRCg7b:CM028485.1

About this gene

This gene has 4 transcripts (splice variants), 242 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010044068.1	CHM-201	2153	685aa	ENSGALP00010026194.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0YYT2	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 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,
ENSGALT00010044082.1	CHM-202	3890	677aa	ENSGALP00010026202.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0Z6K7	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,
ENSGALT00010044092.1	CHM-203	3827	656aa	ENSGALP00010026210.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0Z5K2	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,
ENSGALT00010044075.1	CHM-204	3807	651aa	ENSGALP00010026198.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0Z5J1	-

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Summary

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