Canonical Allele Identifier: CA206882

Gene: ARID1A

Linked Data

• ClinVar Variation Id: 210259
• ClinVar RCV Id: RCV000193411
• dbSNP Id: rs797045263
• gnomAD v4: 1-26696793-TG-T
• MyVariant Identifiers: chr1:g.27023288del (hg19) ; chr1:g.26696797del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696797del , CM000663.2:g.26696797del	GRCh38
NC_000001.10:g.27023288del , CM000663.1:g.27023288del	GRCh37
NC_000001.9:g.26895875del	NCBI36
NG_029965.1:g.5767del , LRG_875:g.5767del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.394del MANE Select	ENSP00000320485.7:p.Val132TrpfsTer?
ENST00000430799.7:c.-13+3180del	ENSP00000390317.3:n.-13+3180del
ENST00000637465.1:c.-13+697del	ENSP00000490650.1:n.-13+697del
ENST00000324856.11:c.394del	ENSP00000320485.7:p.Val132TrpfsTer?
ENST00000457599.6:c.394del	ENSP00000387636.2:p.Val132TrpfsTer?
NM_006015.4:c.394del , LRG_875t1:c.394del	NP_006006.3:p.Val132TrpfsTer?
NM_139135.2:c.394del	NP_624361.1:p.Val132TrpfsTer?
NM_006015.5:c.394del	NP_006006.3:p.Val132TrpfsTer?
NM_139135.3:c.394del	NP_624361.1:p.Val132TrpfsTer?
NM_006015.6:c.394del MANE Select	NP_006006.3:p.Val132TrpfsTer?
NM_139135.4:c.394del	NP_624361.1:p.Val132TrpfsTer?