Canonical Allele Identifier: CA416968008

Gene: ARID1A

Linked Data

• dbSNP Id: rs1212746258
• gnomAD v2: 1-27105645-G-A
• gnomAD v4: 1-26779154-G-A
• MyVariant Identifiers: chr1:g.27105645G>A (hg19) ; chr1:g.26779154G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779154G>A , CM000663.2:g.26779154G>A	GRCh38
NC_000001.10:g.27105645G>A , CM000663.1:g.27105645G>A	GRCh37
NC_000001.9:g.26978232G>A	NCBI36
NG_029965.1:g.88124G>A , LRG_875:g.88124G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5256G>A MANE Select	ENSP00000320485.7:p.Lys1752=
ENST00000374152.7:c.4107G>A	ENSP00000363267.2:p.Lys1369=
ENST00000430799.7:c.4104G>A	ENSP00000390317.3:p.Lys1368=
ENST00000466382.2:c.673G>A
ENST00000636219.1:c.4110G>A	ENSP00000489842.1:p.Lys1370=
ENST00000637788.1:n.1056G>A
ENST00000324856.11:c.5256G>A	ENSP00000320485.7:p.Lys1752=
ENST00000374152.6:c.4107G>A	ENSP00000363267.2:p.Lys1369=
ENST00000430799.6:c.1945G>A
ENST00000457599.6:c.4605G>A	ENSP00000387636.2:p.Lys1535=
ENST00000466382.1:c.673G>A
ENST00000532781.1:c.754G>A
NM_006015.4:c.5256G>A , LRG_875t1:c.5256G>A	NP_006006.3:p.Lys1752=
NM_139135.2:c.4605G>A	NP_624361.1:p.Lys1535=
NM_006015.5:c.5256G>A	NP_006006.3:p.Lys1752=
NM_139135.3:c.4605G>A	NP_624361.1:p.Lys1535=
NM_006015.6:c.5256G>A MANE Select	NP_006006.3:p.Lys1752=
NM_139135.4:c.4605G>A	NP_624361.1:p.Lys1535=