Summary
- Splice variants
- Transcript comparison
- Gene alleles
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Gene: C1H21orf91 ENSBTAG00000001395

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Description

chromosome 1 C21orf91 homolog [Source:VGNC Symbol;Acc:VGNC:52664]

Location

Primary_assembly 1: 19,227,862-19,261,185 forward strand.

ARS-UCD2.0:CM008168.2

About this gene

This gene has 4 transcripts (splice variants) and 201 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000001832.5	C1H21orf91-204	5749	301aa	ENSBTAP00000001832.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6R0W6	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,
ENSBTAT00000142375.1	C1H21orf91-201	5663	297aa	ENSBTAP00000107350.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q32L32	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,
ENSBTAT00000139142.1	C1H21orf91-202	5517	221aa	ENSBTAP00000106360.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S8Y8	-
ENSBTAT00000118042.2	C1H21orf91-203	1655	296aa	ENSBTAP00000088077.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SVN4	APPRIS ALT1: 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 is conserved in at least 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 ALT1,

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Summary

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