Human (GRCh38.p14)
Description

EMG1 N1-specific pseudouridine methyltransferase [Source:HGNC Symbol;Acc:HGNC:16912]

Gene Synonyms

C2F, GRCC2F, NEP1

Location
About this transcript

This transcript has 6 exons, is annotated with 14 domains and features, is associated with 4410 variant alleles and maps to 596 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000599672.6EMG1-2024873244aaENSP00000470560.1
 
Protein coding
CCDS73430Q92979 NM_006331.8MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000539196.2EMG1-201616149aaENSP00000479546.1
 
Protein coding
A0A087WVM7 -TSL:2CDS 5' incomplete
ENST00000611981.1EMG1-2031223No protein-
 
Retained intron
--TSL:2
ENST00000620255.1EMG1-204720No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 6, Coding exons: 6, Transcript length: 4,873 bps, Translation length: 244 residues

MANE

This MANE Select transcript contains ENSP00000470560 and matches to NM_006331.8 and NP_006322.4

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q92979

CCDS

This transcript is a member of the Human CCDS set: CCDS73430

Transcript Support Level (TSL)

TSL:1

Version

ENST00000599672.6

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.

Annotation Attributes

3' standard supported extension [Definitions]

GENCODE basic gene

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