Human (GRCh38.p14)
Description

ArfGAP with dual PH domains 2 [Source:HGNC Symbol;Acc:HGNC:16487]

Gene Synonyms

CENTA2

Location
About this transcript

This transcript has 11 exons, is annotated with 24 domains and features, is associated with 15716 variant alleles and maps to 532 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000330889.8ADAP2-2012669381aaENSP00000329468.3
 
Protein coding
CCDS11261Q9NPF8-1 NM_018404.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT1TSL:1
ENST00000580525.5ADAP2-2041598387aaENSP00000464121.1
 
Protein coding
CCDS86588Q2V6Q1 -GENCODE basicAPPRIS P4TSL:1
ENST00000581285.5ADAP2-2061080333aaENSP00000464155.1
 
Protein coding
J3QRD3 -TSL:3CDS 3' incomplete
ENST00000584828.5ADAP2-209907145aaENSP00000463649.1
 
Protein coding
J3QLP8 -TSL:3CDS 5' incomplete
ENST00000581548.5ADAP2-207584114aaENSP00000467079.1
 
Protein coding
K7ENT1 -TSL:3CDS 3' incomplete
ENST00000584989.1ADAP2-21029698aaENSP00000462634.1
 
Protein coding
J3KST1 -TSL:5CDS 5' and 3' incomplete
ENST00000585130.5ADAP2-2112271106aaENSP00000464120.1
 
Nonsense mediated decay
J3QRA6 -TSL:2
ENST00000580526.1ADAP2-20567684aaENSP00000462832.1
 
Nonsense mediated decay
J3KT70 -TSL:3
ENST00000583688.1ADAP2-208358No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000470962.1ADAP2-202838No protein-
 
Retained intron
--TSL:2
ENST00000480980.1ADAP2-203804No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 11, Coding exons: 11, Transcript length: 2,669 bps, Translation length: 381 residues

MANE

This MANE Select transcript contains ENSP00000329468 and matches to NM_018404.3 and NP_060874.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NPF8

CCDS

This transcript is a member of the Human CCDS set: CCDS11261

Transcript Support Level (TSL)

TSL:1

Version

ENST00000330889.8

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.