Canonical Allele Identifier: CA339184744

Gene: ARID1A

Linked Data

• gnomAD v4: 1-26779219-A-G
• MyVariant Identifiers: chr1:g.27105710A>G (hg19) ; chr1:g.26779219A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779219A>G , CM000663.2:g.26779219A>G	GRCh38
NC_000001.10:g.27105710A>G , CM000663.1:g.27105710A>G	GRCh37
NC_000001.9:g.26978297A>G	NCBI36
NG_029965.1:g.88189A>G , LRG_875:g.88189A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5321A>G MANE Select	ENSP00000320485.7:p.Glu1774Gly
ENST00000374152.7:c.4172A>G	ENSP00000363267.2:p.Glu1391Gly
ENST00000430799.7:c.4169A>G	ENSP00000390317.3:p.Glu1390Gly
ENST00000466382.2:c.738A>G
ENST00000636219.1:c.4175A>G	ENSP00000489842.1:p.Glu1392Gly
ENST00000637788.1:n.1121A>G
ENST00000324856.11:c.5321A>G	ENSP00000320485.7:p.Glu1774Gly
ENST00000374152.6:c.4172A>G	ENSP00000363267.2:p.Glu1391Gly
ENST00000430799.6:c.2010A>G
ENST00000457599.6:c.4670A>G	ENSP00000387636.2:p.Glu1557Gly
ENST00000466382.1:c.738A>G
ENST00000532781.1:c.819A>G
NM_006015.4:c.5321A>G , LRG_875t1:c.5321A>G	NP_006006.3:p.Glu1774Gly
NM_139135.2:c.4670A>G	NP_624361.1:p.Glu1557Gly
NM_006015.5:c.5321A>G	NP_006006.3:p.Glu1774Gly
NM_139135.3:c.4670A>G	NP_624361.1:p.Glu1557Gly
NM_006015.6:c.5321A>G MANE Select	NP_006006.3:p.Glu1774Gly
NM_139135.4:c.4670A>G	NP_624361.1:p.Glu1557Gly