Transcript: ENST00000342415.6 SNRNP48-201

Description

small nuclear ribonucleoprotein U11/U12 subunit 48 [Source:HGNC Symbol;Acc:HGNC:21368]

Gene Synonyms

C6ORF151, DJ336K20B.1, DJ512B11.2, FLJ32234

Location

Chromosome 6: 7,590,198-7,611,967 forward strand.

About this transcript

This transcript has 9 exons, is annotated with 15 domains and features, is associated with 8930 variant alleles and maps to 510 oligo probes.

Gene

This transcript is a product of gene ENSG00000168566.13 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000342415.6	SNRNP48-201	4174	339aa	ENSP00000339834.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS4502	Q6IEG0-1	NM_152551.4	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 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,
ENST00000634363.1	SNRNP48-203	781	149aa	ENSP00000489245.1	Nonsense mediated decay		A0A0U1RQZ2	-	TSL 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs 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:2,
ENST00000496946.1	SNRNP48-202	2610	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	TSL 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs 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:2,

Summary

Statistics

Exons: 9, Coding exons: 9, Transcript length: 4,174 bps, Translation length: 339 residues

MANE

This MANE Select transcript contains ENSP00000339834 and matches to NM_152551.4 and NP_689764.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q6IEG0

CCDS

This transcript is a member of the Human CCDS set: CCDS4502

Transcript Support Level (TSL)

TSL:1

Version

ENST00000342415.6

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: ENST00000342415.6 SNRNP48-201

Summary

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Transcript: ENST00000342415.6 SNRNP48-201

Summary

About Us

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