Canonical Allele Identifier: CA339189201

Gene: ARID1A

Linked Data

• ClinVar Variation Id: 2920687
• ClinVar RCV Id: RCV003647244
• dbSNP Id: rs879255270
• MyVariant Identifiers: chr1:g.27106354C>G (hg19) ; chr1:g.26779863C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779863C>G , CM000663.2:g.26779863C>G	GRCh38
NC_000001.10:g.27106354C>G , CM000663.1:g.27106354C>G	GRCh37
NC_000001.9:g.26978941C>G	NCBI36
NG_029965.1:g.88833C>G , LRG_875:g.88833C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5965C>G MANE Select	ENSP00000320485.7:p.Arg1989Gly
ENST00000374152.7:c.4816C>G	ENSP00000363267.2:p.Arg1606Gly
ENST00000430799.7:c.4813C>G	ENSP00000390317.3:p.Arg1605Gly
ENST00000466382.2:c.1382C>G
ENST00000636219.1:c.4819C>G	ENSP00000489842.1:p.Arg1607Gly
ENST00000637788.1:n.1765C>G
ENST00000324856.11:c.5965C>G	ENSP00000320485.7:p.Arg1989Gly
ENST00000374152.6:c.4816C>G	ENSP00000363267.2:p.Arg1606Gly
ENST00000430799.6:c.2654C>G
ENST00000457599.6:c.5314C>G	ENSP00000387636.2:p.Arg1772Gly
ENST00000466382.1:c.1382C>G
ENST00000532781.1:c.1463C>G
NM_006015.4:c.5965C>G , LRG_875t1:c.5965C>G	NP_006006.3:p.Arg1989Gly
NM_139135.2:c.5314C>G	NP_624361.1:p.Arg1772Gly
NM_006015.5:c.5965C>G	NP_006006.3:p.Arg1989Gly
NM_139135.3:c.5314C>G	NP_624361.1:p.Arg1772Gly
NM_006015.6:c.5965C>G MANE Select	NP_006006.3:p.Arg1989Gly
NM_139135.4:c.5314C>G	NP_624361.1:p.Arg1772Gly