Canonical Allele Identifier: CA339184510

Gene: ARID1A

Linked Data

• MyVariant Identifiers: chr1:g.27105665T>G (hg19) ; chr1:g.26779174T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779174T>G , CM000663.2:g.26779174T>G	GRCh38
NC_000001.10:g.27105665T>G , CM000663.1:g.27105665T>G	GRCh37
NC_000001.9:g.26978252T>G	NCBI36
NG_029965.1:g.88144T>G , LRG_875:g.88144T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5276T>G MANE Select	ENSP00000320485.7:p.Met1759Arg
ENST00000374152.7:c.4127T>G	ENSP00000363267.2:p.Met1376Arg
ENST00000430799.7:c.4124T>G	ENSP00000390317.3:p.Met1375Arg
ENST00000466382.2:c.693T>G
ENST00000636219.1:c.4130T>G	ENSP00000489842.1:p.Met1377Arg
ENST00000637788.1:n.1076T>G
ENST00000324856.11:c.5276T>G	ENSP00000320485.7:p.Met1759Arg
ENST00000374152.6:c.4127T>G	ENSP00000363267.2:p.Met1376Arg
ENST00000430799.6:c.1965T>G
ENST00000457599.6:c.4625T>G	ENSP00000387636.2:p.Met1542Arg
ENST00000466382.1:c.693T>G
ENST00000532781.1:c.774T>G
NM_006015.4:c.5276T>G , LRG_875t1:c.5276T>G	NP_006006.3:p.Met1759Arg
NM_139135.2:c.4625T>G	NP_624361.1:p.Met1542Arg
NM_006015.5:c.5276T>G	NP_006006.3:p.Met1759Arg
NM_139135.3:c.4625T>G	NP_624361.1:p.Met1542Arg
NM_006015.6:c.5276T>G MANE Select	NP_006006.3:p.Met1759Arg
NM_139135.4:c.4625T>G	NP_624361.1:p.Met1542Arg