Canonical Allele Identifier: CA2644294003

Gene: ARID1A

Linked Data

• gnomAD v4: 1-26696411-CGCAGGTCGCCCCCGCCGCCGCCAGCAGCCTGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696415_26696446del , CM000663.2:g.26696415_26696446del	GRCh38
NC_000001.10:g.27022906_27022937del , CM000663.1:g.27022906_27022937del	GRCh37
NC_000001.9:g.26895493_26895524del	NCBI36
NG_029965.1:g.5385_5416del , LRG_875:g.5385_5416del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.12_43del MANE Select	ENSP00000320485.7:p.Val5ProfsTer?
ENST00000430799.7:c.-13+2798_-13+2829del	ENSP00000390317.3:n.-13+2798_-13+2829del
ENST00000637465.1:c.-13+315_-13+346del	ENSP00000490650.1:n.-13+315_-13+346del
ENST00000324856.11:c.12_43del	ENSP00000320485.7:p.Val5ProfsTer?
ENST00000457599.6:c.12_43del	ENSP00000387636.2:p.Val5ProfsTer?
NM_006015.4:c.12_43del , LRG_875t1:c.12_43del	NP_006006.3:p.Val5ProfsTer?
NM_139135.2:c.12_43del	NP_624361.1:p.Val5ProfsTer?
NM_006015.5:c.12_43del	NP_006006.3:p.Val5ProfsTer?
NM_139135.3:c.12_43del	NP_624361.1:p.Val5ProfsTer?
NM_006015.6:c.12_43del MANE Select	NP_006006.3:p.Val5ProfsTer?
NM_139135.4:c.12_43del	NP_624361.1:p.Val5ProfsTer?