Canonical Allele Identifier: CA339184033

Gene: ARID1A

Linked Data

• dbSNP Id: rs2124136725
• MyVariant Identifiers: chr1:g.27105557G>A (hg19) ; chr1:g.26779066G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779066G>A , CM000663.2:g.26779066G>A	GRCh38
NC_000001.10:g.27105557G>A , CM000663.1:g.27105557G>A	GRCh37
NC_000001.9:g.26978144G>A	NCBI36
NG_029965.1:g.88036G>A , LRG_875:g.88036G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5168G>A MANE Select	ENSP00000320485.7:p.Cys1723Tyr
ENST00000374152.7:c.4019G>A	ENSP00000363267.2:p.Cys1340Tyr
ENST00000430799.7:c.4016G>A	ENSP00000390317.3:p.Cys1339Tyr
ENST00000466382.2:c.585G>A
ENST00000636219.1:c.4022G>A	ENSP00000489842.1:p.Cys1341Tyr
ENST00000637788.1:n.968G>A
ENST00000324856.11:c.5168G>A	ENSP00000320485.7:p.Cys1723Tyr
ENST00000374152.6:c.4019G>A	ENSP00000363267.2:p.Cys1340Tyr
ENST00000430799.6:c.1857G>A
ENST00000457599.6:c.4517G>A	ENSP00000387636.2:p.Cys1506Tyr
ENST00000466382.1:c.585G>A
ENST00000532781.1:c.666G>A
NM_006015.4:c.5168G>A , LRG_875t1:c.5168G>A	NP_006006.3:p.Cys1723Tyr
NM_139135.2:c.4517G>A	NP_624361.1:p.Cys1506Tyr
NM_006015.5:c.5168G>A	NP_006006.3:p.Cys1723Tyr
NM_139135.3:c.4517G>A	NP_624361.1:p.Cys1506Tyr
NM_006015.6:c.5168G>A MANE Select	NP_006006.3:p.Cys1723Tyr
NM_139135.4:c.4517G>A	NP_624361.1:p.Cys1506Tyr