Human (GRCh38.p14)
Description

recombination activating 1 [Source:HGNC Symbol;Acc:HGNC:9831]

Gene Synonyms

MGC43321, RNF74

Location
About this transcript

This transcript has 2 exons, is annotated with 22 domains and features, is associated with 5882 variant alleles and maps to 257 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000299440.6RAG1-20165881043aaENSP00000299440.5
 
Protein coding
CCDS7902P15918-1 NM_000448.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000697715.1RAG1-20668811043aaENSP00000513413.1
 
Protein coding
CCDS7902P15918-1 -GENCODE basicAPPRIS P1
ENST00000697713.1RAG1-20467541043aaENSP00000513411.1
 
Protein coding
CCDS7902P15918-1 -GENCODE basicAPPRIS P1
ENST00000697714.1RAG1-20566381043aaENSP00000513412.1
 
Protein coding
CCDS7902P15918-1 -GENCODE basicAPPRIS P1
ENST00000534663.1RAG1-2033707931aaENSP00000434610.1
 
Nonsense mediated decay
P15918-2 -TSL:1
ENST00000529126.5RAG1-202482No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 2, Coding exons: 1, Transcript length: 6,588 bps, Translation length: 1,043 residues

MANE

This MANE Select transcript contains ENSP00000299440 and matches to NM_000448.3 and NP_000439.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: P15918

CCDS

This transcript is a member of the Human CCDS set: CCDS7902

Transcript Support Level (TSL)

TSL:1

Version

ENST00000299440.6

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.