Canonical Allele Identifier: CA339184672

Gene: ARID1A

Linked Data

• dbSNP Id: rs1371234195
• MyVariant Identifiers: chr1:g.27105695T>A (hg19) ; chr1:g.26779204T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779204T>A , CM000663.2:g.26779204T>A	GRCh38
NC_000001.10:g.27105695T>A , CM000663.1:g.27105695T>A	GRCh37
NC_000001.9:g.26978282T>A	NCBI36
NG_029965.1:g.88174T>A , LRG_875:g.88174T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5306T>A MANE Select	ENSP00000320485.7:p.Leu1769Gln
ENST00000374152.7:c.4157T>A	ENSP00000363267.2:p.Leu1386Gln
ENST00000430799.7:c.4154T>A	ENSP00000390317.3:p.Leu1385Gln
ENST00000466382.2:c.723T>A
ENST00000636219.1:c.4160T>A	ENSP00000489842.1:p.Leu1387Gln
ENST00000637788.1:n.1106T>A
ENST00000324856.11:c.5306T>A	ENSP00000320485.7:p.Leu1769Gln
ENST00000374152.6:c.4157T>A	ENSP00000363267.2:p.Leu1386Gln
ENST00000430799.6:c.1995T>A
ENST00000457599.6:c.4655T>A	ENSP00000387636.2:p.Leu1552Gln
ENST00000466382.1:c.723T>A
ENST00000532781.1:c.804T>A
NM_006015.4:c.5306T>A , LRG_875t1:c.5306T>A	NP_006006.3:p.Leu1769Gln
NM_139135.2:c.4655T>A	NP_624361.1:p.Leu1552Gln
NM_006015.5:c.5306T>A	NP_006006.3:p.Leu1769Gln
NM_139135.3:c.4655T>A	NP_624361.1:p.Leu1552Gln
NM_006015.6:c.5306T>A MANE Select	NP_006006.3:p.Leu1769Gln
NM_139135.4:c.4655T>A	NP_624361.1:p.Leu1552Gln