Transcript: ENST00000460212.1 N6AMT1-203

Description

N-6 adenine-specific DNA methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:16021]

Gene Synonyms

C21ORF127, HEMK2, KMT9, MTQ2, N6AMT, PRED28, PRMC

Location

Chromosome 21: 28,872,191-28,885,371 reverse strand.

About this transcript

This transcript has 7 exons, is annotated with 9 domains and features, is associated with 6700 variant alleles and maps to 280 oligo probes.

Gene

This transcript is a product of gene ENSG00000156239.12 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000303775.10	N6AMT1-201	4861	214aa	ENSP00000303584.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS33526	Q9Y5N5-1	NM_013240.6	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,
ENST00000351429.7	N6AMT1-202	4781	186aa	ENSP00000286764.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS33525	Q9Y5N5-2	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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,
ENST00000460212.1	N6AMT1-203	1293	214aa	ENSP00000436490.1	Nonsense mediated decay	CCDS33526	Q9Y5N5-1	-	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,

Summary

Statistics

Exons: 7, Coding exons: 6, Transcript length: 1,293 bps, Translation length: 214 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9Y5N5

CCDS

This transcript is a member of the Human CCDS set: CCDS33526

Transcript Support Level (TSL)

TSL:1

Version

ENST00000460212.1

Type

Nonsense mediated decay

Annotation Method

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

Transcript: ENST00000460212.1 N6AMT1-203

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Transcript: ENST00000460212.1 N6AMT1-203

Summary

About Us

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