Canonical Allele Identifier: CA339184886

Gene: ARID1A

Linked Data

• dbSNP Id: rs2124138382
• MyVariant Identifiers: chr1:g.27105734T>G (hg19) ; chr1:g.26779243T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779243T>G , CM000663.2:g.26779243T>G	GRCh38
NC_000001.10:g.27105734T>G , CM000663.1:g.27105734T>G	GRCh37
NC_000001.9:g.26978321T>G	NCBI36
NG_029965.1:g.88213T>G , LRG_875:g.88213T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5345T>G MANE Select	ENSP00000320485.7:p.Val1782Gly
ENST00000374152.7:c.4196T>G	ENSP00000363267.2:p.Val1399Gly
ENST00000430799.7:c.4193T>G	ENSP00000390317.3:p.Val1398Gly
ENST00000466382.2:c.762T>G
ENST00000636219.1:c.4199T>G	ENSP00000489842.1:p.Val1400Gly
ENST00000637788.1:n.1145T>G
ENST00000324856.11:c.5345T>G	ENSP00000320485.7:p.Val1782Gly
ENST00000374152.6:c.4196T>G	ENSP00000363267.2:p.Val1399Gly
ENST00000430799.6:c.2034T>G
ENST00000457599.6:c.4694T>G	ENSP00000387636.2:p.Val1565Gly
ENST00000466382.1:c.762T>G
ENST00000532781.1:c.843T>G
NM_006015.4:c.5345T>G , LRG_875t1:c.5345T>G	NP_006006.3:p.Val1782Gly
NM_139135.2:c.4694T>G	NP_624361.1:p.Val1565Gly
NM_006015.5:c.5345T>G	NP_006006.3:p.Val1782Gly
NM_139135.3:c.4694T>G	NP_624361.1:p.Val1565Gly
NM_006015.6:c.5345T>G MANE Select	NP_006006.3:p.Val1782Gly
NM_139135.4:c.4694T>G	NP_624361.1:p.Val1565Gly