Canonical Allele Identifier: CA416968013

Gene: ARID1A

Linked Data

• dbSNP Id: rs774970671
• MyVariant Identifiers: chr1:g.27105648G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779157G>C , CM000663.2:g.26779157G>C	GRCh38
NC_000001.10:g.27105648G>C , CM000663.1:g.27105648G>C	GRCh37
NC_000001.9:g.26978235G>C	NCBI36
NG_029965.1:g.88127G>C , LRG_875:g.88127G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5259G>C MANE Select	ENSP00000320485.7:p.Val1753=
ENST00000374152.7:c.4110G>C	ENSP00000363267.2:p.Val1370=
ENST00000430799.7:c.4107G>C	ENSP00000390317.3:p.Val1369=
ENST00000466382.2:c.676G>C
ENST00000636219.1:c.4113G>C	ENSP00000489842.1:p.Val1371=
ENST00000637788.1:n.1059G>C
ENST00000324856.11:c.5259G>C	ENSP00000320485.7:p.Val1753=
ENST00000374152.6:c.4110G>C	ENSP00000363267.2:p.Val1370=
ENST00000430799.6:c.1948G>C
ENST00000457599.6:c.4608G>C	ENSP00000387636.2:p.Val1536=
ENST00000466382.1:c.676G>C
ENST00000532781.1:c.757G>C
NM_006015.4:c.5259G>C , LRG_875t1:c.5259G>C	NP_006006.3:p.Val1753=
NM_139135.2:c.4608G>C	NP_624361.1:p.Val1536=
NM_006015.5:c.5259G>C	NP_006006.3:p.Val1753=
NM_139135.3:c.4608G>C	NP_624361.1:p.Val1536=
NM_006015.6:c.5259G>C MANE Select	NP_006006.3:p.Val1753=
NM_139135.4:c.4608G>C	NP_624361.1:p.Val1536=