Canonical Allele Identifier: CA339184928

Gene: ARID1A

Linked Data

• dbSNP Id: rs1474451753
• MyVariant Identifiers: chr1:g.27105743A>C (hg19) ; chr1:g.26779252A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779252A>C , CM000663.2:g.26779252A>C	GRCh38
NC_000001.10:g.27105743A>C , CM000663.1:g.27105743A>C	GRCh37
NC_000001.9:g.26978330A>C	NCBI36
NG_029965.1:g.88222A>C , LRG_875:g.88222A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5354A>C MANE Select	ENSP00000320485.7:p.Asp1785Ala
ENST00000374152.7:c.4205A>C	ENSP00000363267.2:p.Asp1402Ala
ENST00000430799.7:c.4202A>C	ENSP00000390317.3:p.Asp1401Ala
ENST00000466382.2:c.771A>C
ENST00000636219.1:c.4208A>C	ENSP00000489842.1:p.Asp1403Ala
ENST00000637788.1:n.1154A>C
ENST00000324856.11:c.5354A>C	ENSP00000320485.7:p.Asp1785Ala
ENST00000374152.6:c.4205A>C	ENSP00000363267.2:p.Asp1402Ala
ENST00000430799.6:c.2043A>C
ENST00000457599.6:c.4703A>C	ENSP00000387636.2:p.Asp1568Ala
ENST00000466382.1:c.771A>C
ENST00000532781.1:c.852A>C
NM_006015.4:c.5354A>C , LRG_875t1:c.5354A>C	NP_006006.3:p.Asp1785Ala
NM_139135.2:c.4703A>C	NP_624361.1:p.Asp1568Ala
NM_006015.5:c.5354A>C	NP_006006.3:p.Asp1785Ala
NM_139135.3:c.4703A>C	NP_624361.1:p.Asp1568Ala
NM_006015.6:c.5354A>C MANE Select	NP_006006.3:p.Asp1785Ala
NM_139135.4:c.4703A>C	NP_624361.1:p.Asp1568Ala