Canonical Allele Identifier: CA416968030

Gene: ARID1A

Linked Data

• MyVariant Identifiers: chr1:g.27105657A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779166A>C , CM000663.2:g.26779166A>C	GRCh38
NC_000001.10:g.27105657A>C , CM000663.1:g.27105657A>C	GRCh37
NC_000001.9:g.26978244A>C	NCBI36
NG_029965.1:g.88136A>C , LRG_875:g.88136A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5268A>C MANE Select	ENSP00000320485.7:p.Pro1756=
ENST00000374152.7:c.4119A>C	ENSP00000363267.2:p.Pro1373=
ENST00000430799.7:c.4116A>C	ENSP00000390317.3:p.Pro1372=
ENST00000466382.2:c.685A>C
ENST00000636219.1:c.4122A>C	ENSP00000489842.1:p.Pro1374=
ENST00000637788.1:n.1068A>C
ENST00000324856.11:c.5268A>C	ENSP00000320485.7:p.Pro1756=
ENST00000374152.6:c.4119A>C	ENSP00000363267.2:p.Pro1373=
ENST00000430799.6:c.1957A>C
ENST00000457599.6:c.4617A>C	ENSP00000387636.2:p.Pro1539=
ENST00000466382.1:c.685A>C
ENST00000532781.1:c.766A>C
NM_006015.4:c.5268A>C , LRG_875t1:c.5268A>C	NP_006006.3:p.Pro1756=
NM_139135.2:c.4617A>C	NP_624361.1:p.Pro1539=
NM_006015.5:c.5268A>C	NP_006006.3:p.Pro1756=
NM_139135.3:c.4617A>C	NP_624361.1:p.Pro1539=
NM_006015.6:c.5268A>C MANE Select	NP_006006.3:p.Pro1756=
NM_139135.4:c.4617A>C	NP_624361.1:p.Pro1539=