Summary
Sequence
Protein Information
- Protein summary
- Domains & features
- Variants
- PDB 3D protein model
- AlphaFold predicted model
Genetic Variation
External References
- General identifiers
- Oligo probes
Supporting evidence
ID History
- Transcript history
- Protein history

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Transcript: ENSRNOT00000089611.2 Sesn1-202

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Description

sestrin 1 [Source:RGD Symbol;Acc:1307517]

Gene Synonyms

LOC294518

Location

Primary_assembly 20: 45,294,871-45,387,694 forward strand.

About this transcript

This transcript has 10 exons, is annotated with 7 domains and features, is associated with 342 variant alleles and maps to 193 oligo probes.

Gene

This transcript is a product of gene ENSRNOG00000000302.8 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000089611.2	Sesn1-202	3457	551aa	ENSRNOP00000073119.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K4P1	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 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,
ENSRNOT00000065890.2	Sesn1-201	2850	462aa	ENSRNOP00000060435.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZJU4	-
ENSRNOT00000116987.1	Sesn1-203	2616	492aa	ENSRNOP00000090761.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AEX8	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,

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Protein summary

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Protein domains for ENSRNOP00000073119.1

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