Transcript: ENST00000609256.2 BHLHA15-202

Description

basic helix-loop-helix family member a15 [Source:HGNC Symbol;Acc:HGNC:22265]

Gene Synonyms

BHLHB8, MIST1

Location

Chromosome 7: 98,211,439-98,215,457 forward strand.

About this transcript

This transcript has 2 exons, is annotated with 15 domains and features, is associated with 2135 variant alleles and maps to 254 oligo probes.

Gene

This transcript is a product of gene ENSG00000180535.4 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000609256.2	BHLHA15-202	3262	189aa	ENSP00000476312.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS5655	Q7RTS1	NM_177455.4	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, 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, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1, TSL 3: A transcript where the only support is from a single EST The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:3,
ENST00000314018.2	BHLHA15-201	706	189aa	ENSP00000326391.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS5655	Q7RTS1	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1, TSL NA: A transcript that was not analysed for TSL. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:NA,

Summary

Statistics

Exons: 2, Coding exons: 1, Transcript length: 3,262 bps, Translation length: 189 residues

MANE

This MANE Select transcript contains ENSP00000476312 and matches to NM_177455.4 and NP_803238.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q7RTS1

CCDS

This transcript is a member of the Human CCDS set: CCDS5655

Transcript Support Level (TSL)

TSL:3

Version

ENST00000609256.2

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Annotation Attributes

not organism-supported [Definitions]

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

Transcript: ENST00000609256.2 BHLHA15-202

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Transcript: ENST00000609256.2 BHLHA15-202

Summary

About Us

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