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 27774 variant alleles and maps to 233 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: 6,638 bps, Translation length: 1,043 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P15918

CCDS

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

Version

ENST00000697714.1

Type

Protein coding

Annotation Method

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

Annotation Attributes

inferred transcript model [Definitions]

RNA-Seq supported only

GENCODE basic gene

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