Canonical Allele Identifier: CA15081607

Gene: ARID1A

Linked Data

• dbSNP Id: rs11247593
• gnomAD v2: 1-27052080-G-A
• gnomAD v3: 1-26725589-G-A
• gnomAD v4: 1-26725589-G-A
• MyVariant Identifiers: chr1:g.27052080G>A (hg19) ; chr1:g.26725589G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26725589G>A , CM000663.2:g.26725589G>A	GRCh38
NC_000001.10:g.27052080G>A , CM000663.1:g.27052080G>A	GRCh37
NC_000001.9:g.26924667G>A	NCBI36
NG_029965.1:g.34559G>A , LRG_875:g.34559G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.1138-4062G>A MANE Select	ENSP00000320485.7:n.1138-4062G>A
ENST00000430799.7:c.-12-4062G>A	ENSP00000390317.3:n.-12-4062G>A
ENST00000637465.1:c.-12-4062G>A	ENSP00000490650.1:n.-12-4062G>A
ENST00000324856.11:c.1138-4062G>A	ENSP00000320485.7:n.1138-4062G>A
ENST00000457599.6:c.1138-4062G>A	ENSP00000387636.2:n.1138-4062G>A
NM_006015.4:c.1138-4062G>A , LRG_875t1:c.1138-4062G>A	NP_006006.3:n.1138-4062G>A
NM_139135.2:c.1138-4062G>A	NP_624361.1:n.1138-4062G>A
NM_006015.5:c.1138-4062G>A	NP_006006.3:n.1138-4062G>A
NM_139135.3:c.1138-4062G>A	NP_624361.1:n.1138-4062G>A
NM_006015.6:c.1138-4062G>A MANE Select	NP_006006.3:n.1138-4062G>A
NM_139135.4:c.1138-4062G>A	NP_624361.1:n.1138-4062G>A