Canonical Allele Identifier: CA339184476

Gene: ARID1A

Linked Data

• dbSNP Id: rs2124137643
• MyVariant Identifiers: chr1:g.27105656C>A (hg19) ; chr1:g.26779165C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779165C>A , CM000663.2:g.26779165C>A	GRCh38
NC_000001.10:g.27105656C>A , CM000663.1:g.27105656C>A	GRCh37
NC_000001.9:g.26978243C>A	NCBI36
NG_029965.1:g.88135C>A , LRG_875:g.88135C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5267C>A MANE Select	ENSP00000320485.7:p.Pro1756Gln
ENST00000374152.7:c.4118C>A	ENSP00000363267.2:p.Pro1373Gln
ENST00000430799.7:c.4115C>A	ENSP00000390317.3:p.Pro1372Gln
ENST00000466382.2:c.684C>A
ENST00000636219.1:c.4121C>A	ENSP00000489842.1:p.Pro1374Gln
ENST00000637788.1:n.1067C>A
ENST00000324856.11:c.5267C>A	ENSP00000320485.7:p.Pro1756Gln
ENST00000374152.6:c.4118C>A	ENSP00000363267.2:p.Pro1373Gln
ENST00000430799.6:c.1956C>A
ENST00000457599.6:c.4616C>A	ENSP00000387636.2:p.Pro1539Gln
ENST00000466382.1:c.684C>A
ENST00000532781.1:c.765C>A
NM_006015.4:c.5267C>A , LRG_875t1:c.5267C>A	NP_006006.3:p.Pro1756Gln
NM_139135.2:c.4616C>A	NP_624361.1:p.Pro1539Gln
NM_006015.5:c.5267C>A	NP_006006.3:p.Pro1756Gln
NM_139135.3:c.4616C>A	NP_624361.1:p.Pro1539Gln
NM_006015.6:c.5267C>A MANE Select	NP_006006.3:p.Pro1756Gln
NM_139135.4:c.4616C>A	NP_624361.1:p.Pro1539Gln