Canonical Allele Identifier: CA339184968

Gene: ARID1A

Linked Data

• dbSNP Id: rs2124138573
• MyVariant Identifiers: chr1:g.27105750G>C (hg19) ; chr1:g.26779259G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779259G>C , CM000663.2:g.26779259G>C	GRCh38
NC_000001.10:g.27105750G>C , CM000663.1:g.27105750G>C	GRCh37
NC_000001.9:g.26978337G>C	NCBI36
NG_029965.1:g.88229G>C , LRG_875:g.88229G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5361G>C MANE Select	ENSP00000320485.7:p.Glu1787Asp
ENST00000374152.7:c.4212G>C	ENSP00000363267.2:p.Glu1404Asp
ENST00000430799.7:c.4209G>C	ENSP00000390317.3:p.Glu1403Asp
ENST00000466382.2:c.778G>C
ENST00000636219.1:c.4215G>C	ENSP00000489842.1:p.Glu1405Asp
ENST00000637788.1:n.1161G>C
ENST00000324856.11:c.5361G>C	ENSP00000320485.7:p.Glu1787Asp
ENST00000374152.6:c.4212G>C	ENSP00000363267.2:p.Glu1404Asp
ENST00000430799.6:c.2050G>C
ENST00000457599.6:c.4710G>C	ENSP00000387636.2:p.Glu1570Asp
ENST00000466382.1:c.778G>C
ENST00000532781.1:c.859G>C
NM_006015.4:c.5361G>C , LRG_875t1:c.5361G>C	NP_006006.3:p.Glu1787Asp
NM_139135.2:c.4710G>C	NP_624361.1:p.Glu1570Asp
NM_006015.5:c.5361G>C	NP_006006.3:p.Glu1787Asp
NM_139135.3:c.4710G>C	NP_624361.1:p.Glu1570Asp
NM_006015.6:c.5361G>C MANE Select	NP_006006.3:p.Glu1787Asp
NM_139135.4:c.4710G>C	NP_624361.1:p.Glu1570Asp