Canonical Allele Identifier: CA19815149

Gene: ARID1A

Linked Data

• dbSNP Id: rs775549195
• gnomAD v4: 1-26779168-C-A
• MyVariant Identifiers: chr1:g.27105659C>A (hg19) ; chr1:g.26779168C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779168C>A , CM000663.2:g.26779168C>A	GRCh38
NC_000001.10:g.27105659C>A , CM000663.1:g.27105659C>A	GRCh37
NC_000001.9:g.26978246C>A	NCBI36
NG_029965.1:g.88138C>A , LRG_875:g.88138C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5270C>A MANE Select	ENSP00000320485.7:p.Ala1757Asp
ENST00000374152.7:c.4121C>A	ENSP00000363267.2:p.Ala1374Asp
ENST00000430799.7:c.4118C>A	ENSP00000390317.3:p.Ala1373Asp
ENST00000466382.2:c.687C>A
ENST00000636219.1:c.4124C>A	ENSP00000489842.1:p.Ala1375Asp
ENST00000637788.1:n.1070C>A
ENST00000324856.11:c.5270C>A	ENSP00000320485.7:p.Ala1757Asp
ENST00000374152.6:c.4121C>A	ENSP00000363267.2:p.Ala1374Asp
ENST00000430799.6:c.1959C>A
ENST00000457599.6:c.4619C>A	ENSP00000387636.2:p.Ala1540Asp
ENST00000466382.1:c.687C>A
ENST00000532781.1:c.768C>A
NM_006015.4:c.5270C>A , LRG_875t1:c.5270C>A	NP_006006.3:p.Ala1757Asp
NM_139135.2:c.4619C>A	NP_624361.1:p.Ala1540Asp
NM_006015.5:c.5270C>A	NP_006006.3:p.Ala1757Asp
NM_139135.3:c.4619C>A	NP_624361.1:p.Ala1540Asp
NM_006015.6:c.5270C>A MANE Select	NP_006006.3:p.Ala1757Asp
NM_139135.4:c.4619C>A	NP_624361.1:p.Ala1540Asp