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Human (GRCh38.p14)
Description

deleted in azoospermia 3 [Source:HGNC Symbol;Acc:HGNC:15965]

Location
About this transcript

This transcript has 19 exons, is annotated with 33 domains and features, is associated with 312 variant alleles and maps to 2424 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000382365.7DAZ3-2023417438aaENSP00000371802.2
 
Protein coding
CCDS35489Q9NR90-2 NM_020364.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS ALT2TSL:1
ENST00000446723.4DAZ3-2033372390aaENSP00000401049.1
 
Protein coding
E7ERQ6 -GENCODE PrimaryGENCODE BasicAPPRIS P2TSL:1
ENST00000315357.9DAZ3-2013277366aaENSP00000324965.7
 
Protein coding
E7ETR3 -GENCODE PrimaryGENCODE BasicAPPRIS ALT2TSL:1
ENST00000692367.1DAZ3-2052242No protein-
 
Protein coding CDS not defined
---
ENST00000691059.1DAZ3-2041502No protein-
 
Protein coding CDS not defined
---
Statistics

Exons: 19, Coding exons: 18, Transcript length: 3,417 bps, Translation length: 438 residues

MANE

This MANE Select transcript contains ENSP00000371802 and matches to NM_020364.4 and NP_065097.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NR90

CCDS

This transcript is a member of the Human CCDS set: CCDS35489

Transcript Support Level (TSL)

TSL:1

Version

ENST00000382365.7

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.

GENCODE primary gene

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