Canonical Allele Identifier: CA416968220

Gene: ARID1A

Linked Data

• dbSNP Id: rs2081167020
• gnomAD v3: 1-26779238-A-G
• gnomAD v4: 1-26779238-A-G
• MyVariant Identifiers: chr1:g.27105729A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779238A>G , CM000663.2:g.26779238A>G	GRCh38
NC_000001.10:g.27105729A>G , CM000663.1:g.27105729A>G	GRCh37
NC_000001.9:g.26978316A>G	NCBI36
NG_029965.1:g.88208A>G , LRG_875:g.88208A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5340A>G MANE Select	ENSP00000320485.7:p.Glu1780=
ENST00000374152.7:c.4191A>G	ENSP00000363267.2:p.Glu1397=
ENST00000430799.7:c.4188A>G	ENSP00000390317.3:p.Glu1396=
ENST00000466382.2:c.757A>G
ENST00000636219.1:c.4194A>G	ENSP00000489842.1:p.Glu1398=
ENST00000637788.1:n.1140A>G
ENST00000324856.11:c.5340A>G	ENSP00000320485.7:p.Glu1780=
ENST00000374152.6:c.4191A>G	ENSP00000363267.2:p.Glu1397=
ENST00000430799.6:c.2029A>G
ENST00000457599.6:c.4689A>G	ENSP00000387636.2:p.Glu1563=
ENST00000466382.1:c.757A>G
ENST00000532781.1:c.838A>G
NM_006015.4:c.5340A>G , LRG_875t1:c.5340A>G	NP_006006.3:p.Glu1780=
NM_139135.2:c.4689A>G	NP_624361.1:p.Glu1563=
NM_006015.5:c.5340A>G	NP_006006.3:p.Glu1780=
NM_139135.3:c.4689A>G	NP_624361.1:p.Glu1563=
NM_006015.6:c.5340A>G MANE Select	NP_006006.3:p.Glu1780=
NM_139135.4:c.4689A>G	NP_624361.1:p.Glu1563=