Human (GRCh38.p14)
Description

AT-rich interaction domain 2 [Source:HGNC Symbol;Acc:HGNC:18037]

Gene Synonyms

BAF200, DKFZP686G052, FLJ30619, KIAA1557, SMARCF3

Location

Chromosome 12: 45,729,706-45,908,040 forward strand.

GRCh38:CM000674.2

About this gene

This gene has 10 transcripts (splice variants), 219 orthologues and is associated with 100 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000334344.11ARID2-20185981835aaENSP00000335044.6
 
Protein coding
CCDS31783Q68CP9-1 NM_152641.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000444670.5ARID2-20573161451aaENSP00000397307.2
 
Protein coding
F8W108 -TSL:1CDS 5' incomplete
ENST00000422737.7ARID2-20256911788aaENSP00000415650.3
 
Protein coding
F8WCU9 -GENCODE basicTSL:1
ENST00000457135.2ARID2-2064736530aaENSP00000388357.3
 
Protein coding
F8VWP4 -TSL:1CDS 5' incomplete
ENST00000477947.1ARID2-20752364aaENSP00000481488.1
 
Protein coding
A0A087WY37 -TSL:3CDS 5' incomplete
ENST00000479608.5ARID2-2087761246aaENSP00000514783.1
 
Nonsense mediated decay
A0A8V8TP93 -TSL:1CDS 5' incomplete
ENST00000700074.1ARID2-210735No protein-
 
Protein coding CDS not defined
---
ENST00000426776.5ARID2-203484No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000427628.5ARID2-204323No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000480128.1ARID2-2093260No protein-
 
Retained intron
--TSL:2