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

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Gene: CTSG ENSG00000100448

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Description

cathepsin G [Source:HGNC Symbol;Acc:2532]

Gene Synonyms

CATG, CG

Location

Chromosome 14: 25,042,728-25,045,466 reverse strand.

GRCh37:CM000676.1

About this gene

This gene has 2 transcripts (splice variants) and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000216336.2	CTSG-001	886	255aa	ENSP00000216336.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS9631	P08311	NM_001911.2	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,
ENST00000552252.1	CTSG-002	1364	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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