Canonical Allele Identifier: CA339184690

Gene: ARID1A

Linked Data

• ClinVar Variation Id: 975335
• ClinVar RCV Id: RCV001251894
• dbSNP Id: rs747674955
• MyVariant Identifiers: chr1:g.27105698G>A (hg19) ; chr1:g.26779207G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779207G>A , CM000663.2:g.26779207G>A	GRCh38
NC_000001.10:g.27105698G>A , CM000663.1:g.27105698G>A	GRCh37
NC_000001.9:g.26978285G>A	NCBI36
NG_029965.1:g.88177G>A , LRG_875:g.88177G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5309G>A MANE Select	ENSP00000320485.7:p.Gly1770Asp
ENST00000374152.7:c.4160G>A	ENSP00000363267.2:p.Gly1387Asp
ENST00000430799.7:c.4157G>A	ENSP00000390317.3:p.Gly1386Asp
ENST00000466382.2:c.726G>A
ENST00000636219.1:c.4163G>A	ENSP00000489842.1:p.Gly1388Asp
ENST00000637788.1:n.1109G>A
ENST00000324856.11:c.5309G>A	ENSP00000320485.7:p.Gly1770Asp
ENST00000374152.6:c.4160G>A	ENSP00000363267.2:p.Gly1387Asp
ENST00000430799.6:c.1998G>A
ENST00000457599.6:c.4658G>A	ENSP00000387636.2:p.Gly1553Asp
ENST00000466382.1:c.726G>A
ENST00000532781.1:c.807G>A
NM_006015.4:c.5309G>A , LRG_875t1:c.5309G>A	NP_006006.3:p.Gly1770Asp
NM_139135.2:c.4658G>A	NP_624361.1:p.Gly1553Asp
NM_006015.5:c.5309G>A	NP_006006.3:p.Gly1770Asp
NM_139135.3:c.4658G>A	NP_624361.1:p.Gly1553Asp
NM_006015.6:c.5309G>A MANE Select	NP_006006.3:p.Gly1770Asp
NM_139135.4:c.4658G>A	NP_624361.1:p.Gly1553Asp