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

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Transcript: ENSBTAT00000030514.6 ATG2B-201

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Description

autophagy related 2B [Source:VGNC Symbol;Acc:VGNC:26255]

Location

Primary_assembly 21: 61,171,215-61,248,624 reverse strand.

About this transcript

This transcript has 41 exons, is annotated with 15 domains and features, is associated with 4653 variant alleles and maps to 12 oligo probes.

Gene

This transcript is a product of gene ENSBTAG00000012833.7 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000107623.1	ATG2B-202	7644	2127aa	ENSBTAP00000086093.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SST7	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,
ENSBTAT00000113252.1	ATG2B-203	7515	2084aa	ENSBTAP00000077301.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RXM9	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,
ENSBTAT00000030514.6	ATG2B-201	7176	1971aa	ENSBTAP00000030494.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BH30	-

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Protein summary

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Protein domains for ENSBTAP00000030494.6

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