Canonical Allele Identifier: CA2644294016

Gene: ARID1A

Linked Data

• gnomAD v4: 1-26696432-C-CCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696437_26696439dup , CM000663.2:g.26696437_26696439dup	GRCh38
NC_000001.10:g.27022928_27022930dup , CM000663.1:g.27022928_27022930dup	GRCh37
NC_000001.9:g.26895515_26895517dup	NCBI36
NG_029965.1:g.5407_5409dup , LRG_875:g.5407_5409dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.34_36dup MANE Select	ENSP00000320485.7:p.Ser12_Leu13insSer
ENST00000430799.7:c.-13+2820_-13+2822dup	ENSP00000390317.3:n.-13+2820_-13+2822dup
ENST00000637465.1:c.-13+337_-13+339dup	ENSP00000490650.1:n.-13+337_-13+339dup
ENST00000324856.11:c.34_36dup	ENSP00000320485.7:p.Ser12_Leu13insSer
ENST00000457599.6:c.34_36dup	ENSP00000387636.2:p.Ser12_Leu13insSer
NM_006015.4:c.34_36dup , LRG_875t1:c.34_36dup	NP_006006.3:p.Ser12_Leu13insSer
NM_139135.2:c.34_36dup	NP_624361.1:p.Ser12_Leu13insSer
NM_006015.5:c.34_36dup	NP_006006.3:p.Ser12_Leu13insSer
NM_139135.3:c.34_36dup	NP_624361.1:p.Ser12_Leu13insSer
NM_006015.6:c.34_36dup MANE Select	NP_006006.3:p.Ser12_Leu13insSer
NM_139135.4:c.34_36dup	NP_624361.1:p.Ser12_Leu13insSer