Transcript: ENST00000374662.4 HSD17B8-203

Description

hydroxysteroid 17-beta dehydrogenase 8 [Source:HGNC Symbol;Acc:HGNC:3554]

Gene Synonyms

D6S2245E, FABGL, H2-KE6, HKE6, KE6, RING2, SDR30C1

Location

Chromosome 6: 33,204,655-33,206,831 forward strand.

About this transcript

This transcript has 9 exons, is annotated with 36 domains and features, is associated with 1202 variant alleles and maps to 1398 oligo probes.

Gene

This transcript is a product of gene ENSG00000204228.4 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000374662.4	HSD17B8-203	977	261aa	ENSP00000363794.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS4769	A0A1U9X7U3 Q92506	NM_014234.5	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 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. 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:1,
ENST00000469186.1	HSD17B8-204	933	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-	TSL 5: A transcript where no single transcript supports the model structure. 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:5,

Summary

Statistics

Exons: 9, Coding exons: 9, Transcript length: 977 bps, Translation length: 261 residues

MANE

This MANE Select transcript contains ENSP00000363794 and matches to NM_014234.5 and NP_055049.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q92506

CCDS

This transcript is a member of the Human CCDS set: CCDS4769

Transcript Support Level (TSL)

TSL:1

Version

ENST00000374662.4

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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

Transcript: ENST00000374662.4 HSD17B8-203

Summary

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Transcript: ENST00000374662.4 HSD17B8-203

Summary

About Us

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