Canonical Allele Identifier: CA521909929

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696463_26696465dup , CM000663.2:g.26696463_26696465dup	GRCh38
NC_000001.10:g.27022954_27022956dup , CM000663.1:g.27022954_27022956dup	GRCh37
NC_000001.9:g.26895541_26895543dup	NCBI36
NG_029965.1:g.5433_5435dup , LRG_875:g.5433_5435dup

Transcript Alleles

HGVS	Amino-acid Change
NM_006015.6:c.60_62dup MANE Select	NP_006006.3:p.Pro21_Ser22insPro
ENST00000324856.13:c.60_62dup MANE Select	ENSP00000320485.7:p.Pro21_Ser22insPro
NM_006015.4:c.60_62dup , LRG_875t1:c.60_62dup	NP_006006.3:p.Pro21_Ser22insPro
NM_006015.5:c.60_62dup	NP_006006.3:p.Pro21_Ser22insPro
NM_139135.2:c.60_62dup	NP_624361.1:p.Pro21_Ser22insPro
NM_139135.3:c.60_62dup	NP_624361.1:p.Pro21_Ser22insPro
NM_139135.4:c.60_62dup	NP_624361.1:p.Pro21_Ser22insPro
ENST00000324856.11:c.60_62dup	ENSP00000320485.7:p.Pro21_Ser22insPro
ENST00000430799.7:c.-13+2846_-13+2848dup	ENSP00000390317.3:n.-13+2846_-13+2848dup
ENST00000457599.6:c.60_62dup	ENSP00000387636.2:p.Pro21_Ser22insPro
ENST00000637465.1:c.-13+363_-13+365dup	ENSP00000490650.1:n.-13+363_-13+365dup