Human (GRCh38.p14)
Description

tRNA methyltransferase 13 homolog [Source:HGNC Symbol;Acc:HGNC:25502]

Gene Synonyms

CCDC76, FLJ10287, FLJ11219

About this transcript

This transcript has 11 exons, is annotated with 10 domains and features, is associated with 6775 variant alleles and maps to 468 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000370141.8TRMT13-2023128481aaENSP00000359160.2
 
Protein coding
CCDS765Q9NUP7-1 NM_019083.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000370139.1TRMT13-201711130aaENSP00000359158.1
 
Protein coding
Q5VVK9 -GENCODE basicTSL:3
ENST00000370143.5TRMT13-203476109aaENSP00000359162.1
 
Protein coding
Q5VVL2 -GENCODE basicTSL:3
ENST00000482437.5TRMT13-2041582175aaENSP00000432616.1
 
Nonsense mediated decay
Q9NUP7-2 -TSL:2
ENST00000493651.1TRMT13-205586No protein-
 
Protein coding CDS not defined
--TSL:2
Statistics

Exons: 11, Coding exons: 11, Transcript length: 3,128 bps, Translation length: 481 residues

MANE

This MANE Select transcript contains ENSP00000359160 and matches to NM_019083.3 and NP_061956.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NUP7

CCDS

This transcript is a member of the Human CCDS set: CCDS765

Transcript Support Level (TSL)

TSL:1

Version

ENST00000370141.8

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.