Human (GRCh38.p14)
Description

CDV3 homolog [Source:HGNC Symbol;Acc:HGNC:26928]

Gene Synonyms

H41

About this transcript

This transcript has 5 exons, is annotated with 13 domains and features, is associated with 8497 variant alleles and maps to 543 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000264993.8CDV3-2013351258aaENSP00000264993.3
 
Protein coding
CCDS3079Q9UKY7-1 NM_017548.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P3TSL:1
ENST00000420115.6CDV3-2023621110aaENSP00000413272.2
 
Protein coding
CCDS46918Q9UKY7-3 -GENCODE basicTSL:2
ENST00000688838.1CDV3-2103348257aaENSP00000508628.1
 
Protein coding
CCDS93387A0A8I5KX85 -GENCODE basicAPPRIS ALT1
ENST00000515421.1CDV3-2091305108aaENSP00000421495.1
 
Protein coding
CCDS75014D6RFH2 -GENCODE basicTSL:3
ENST00000431519.6CDV3-203955213aaENSP00000391955.2
 
Protein coding
CCDS46917Q9UKY7-2 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000508481.5CDV3-207661156aaENSP00000422866.1
 
Protein coding
CCDS75013D6R9V8 -GENCODE basicTSL:3
ENST00000511392.5CDV3-208554108aaENSP00000425297.1
 
Protein coding
CCDS75015D6RDN0 -GENCODE basicTSL:5
ENST00000504867.5CDV3-20547153aaENSP00000423349.1
 
Protein coding
D6R973 -TSL:3CDS 3' incomplete
ENST00000507408.5CDV3-20644892aaENSP00000424742.1
 
Protein coding
D6RAV0 -TSL:2CDS 3' incomplete
ENST00000503932.6CDV3-20459848aaENSP00000421340.2
 
Nonsense mediated decay
H0Y8K3 -TSL:4
Statistics

Exons: 5, Coding exons: 5, Transcript length: 3,351 bps, Translation length: 258 residues

MANE

This MANE Select transcript contains ENSP00000264993 and matches to NM_017548.5 and NP_060018.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UKY7

CCDS

This transcript is a member of the Human CCDS set: CCDS3079

Transcript Support Level (TSL)

TSL:1

Version

ENST00000264993.8

Type

Protein coding

Annotation Method

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

GENCODE basic gene

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