Human (GRCh38.p14)
Description

retinoic acid induced 2 [Source:HGNC Symbol;Acc:HGNC:9835]

Location
About this transcript

This transcript has 3 exons, is annotated with 5 domains and features, is associated with 17382 variant alleles and maps to 276 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000451717.6RAI2-2042187530aaENSP00000401323.1
 
Protein coding
CCDS14183Q9Y5P3-1 NM_021785.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000545871.1RAI2-2062421530aaENSP00000444210.1
 
Protein coding
CCDS14183Q9Y5P3-1 -GENCODE basicAPPRIS P1TSL:4
ENST00000360011.5RAI2-2022377530aaENSP00000353106.1
 
Protein coding
CCDS14183Q9Y5P3-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000331511.5RAI2-2012317530aaENSP00000333456.1
 
Protein coding
CCDS14183Q9Y5P3-1 -GENCODE basicAPPRIS P1TSL:2
ENST00000415486.7RAI2-2032037480aaENSP00000392578.2
 
Protein coding
CCDS55374Q9Y5P3-2 -GENCODE basicTSL:2
ENST00000509491.2RAI2-20546381aaENSP00000473562.1
 
Protein coding
R4GNA9 -TSL:3CDS 3' incomplete
Statistics

Exons: 3, Coding exons: 2, Transcript length: 2,037 bps, Translation length: 480 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9Y5P3

CCDS

This transcript is a member of the Human CCDS set: CCDS55374

Transcript Support Level (TSL)

TSL:2

Version

ENST00000415486.7

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.