Human (GRCh38.p14)
Description

CHD9 neighbor [Source:HGNC Symbol;Acc:HGNC:53436]

Gene Synonyms

PR-LNCRNA-1

Location
About this transcript

This transcript has 3 exons, is annotated with 6 domains and features, is associated with 4976 variant alleles and maps to 335 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000619363.3CHD9NB-202299652aaENSP00000490424.1
 
Protein coding
CCDS92160A0A1B0GV96 NM_001396020.1MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:5
ENST00000946301.1CHD9NB-204140552aaENSP00000616360.1
 
Protein coding
CCDS92160--GENCODE BasicAPPRIS P1
ENST00000946302.1CHD9NB-205128152aaENSP00000616361.1
 
Protein coding
CCDS92160--GENCODE BasicAPPRIS P1
ENST00000937481.1CHD9NB-203125452aaENSP00000607540.1
 
Protein coding
CCDS92160--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000562178.1CHD9NB-201464No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 3, Coding exons: 1, Transcript length: 2,996 bps, Translation length: 52 residues

MANE

This MANE Select transcript contains ENSP00000490424 and matches to NM_001396020.1 and NP_001382949.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: A0A1B0GV96

CCDS

This transcript is a member of the Human CCDS set: CCDS92160

Transcript Support Level (TSL)

TSL:5

Version

ENST00000619363.3

Type

Protein coding

Annotation Method

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

Annotation Attributes

CAGE supported TSS [Definitions]

GENCODE basic gene

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

GENCODE primary gene

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