Canonical Allele Identifier: CA2644294059

Gene: ARID1A

Linked Data

• gnomAD v4: 1-26696594-GGCCGCCGCAGCCGCTGGGAAAGGAGCTGCAGGACGGGGCCGAGAGCAATGGGGGTGGCGGCGGCGGCGGAGCCGGCAGCGGCGGCGGGCCCGGCGCGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696599_26696697del , CM000663.2:g.26696599_26696697del	GRCh38
NC_000001.10:g.27023090_27023188del , CM000663.1:g.27023090_27023188del	GRCh37
NC_000001.9:g.26895677_26895775del	NCBI36
NG_029965.1:g.5569_5667del , LRG_875:g.5569_5667del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.196_294del MANE Select	ENSP00000320485.7:p.Pro66_Pro98del
ENST00000430799.7:c.-13+2982_-13+3080del	ENSP00000390317.3:n.-13+2982_-13+3080del
ENST00000637465.1:c.-13+499_-13+597del	ENSP00000490650.1:n.-13+499_-13+597del
ENST00000324856.11:c.196_294del	ENSP00000320485.7:p.Pro66_Pro98del
ENST00000457599.6:c.196_294del	ENSP00000387636.2:p.Pro66_Pro98del
NM_006015.4:c.196_294del , LRG_875t1:c.196_294del	NP_006006.3:p.Pro66_Pro98del
NM_139135.2:c.196_294del	NP_624361.1:p.Pro66_Pro98del
NM_006015.5:c.196_294del	NP_006006.3:p.Pro66_Pro98del
NM_139135.3:c.196_294del	NP_624361.1:p.Pro66_Pro98del
NM_006015.6:c.196_294del MANE Select	NP_006006.3:p.Pro66_Pro98del
NM_139135.4:c.196_294del	NP_624361.1:p.Pro66_Pro98del