Canonical Allele Identifier: CA416968005

Gene: ARID1A

Linked Data

• dbSNP Id: rs1279351877
• MyVariant Identifiers: chr1:g.27105642C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779151C>T , CM000663.2:g.26779151C>T	GRCh38
NC_000001.10:g.27105642C>T , CM000663.1:g.27105642C>T	GRCh37
NC_000001.9:g.26978229C>T	NCBI36
NG_029965.1:g.88121C>T , LRG_875:g.88121C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5253C>T MANE Select	ENSP00000320485.7:p.Ser1751=
ENST00000374152.7:c.4104C>T	ENSP00000363267.2:p.Ser1368=
ENST00000430799.7:c.4101C>T	ENSP00000390317.3:p.Ser1367=
ENST00000466382.2:c.670C>T
ENST00000636219.1:c.4107C>T	ENSP00000489842.1:p.Ser1369=
ENST00000637788.1:n.1053C>T
ENST00000324856.11:c.5253C>T	ENSP00000320485.7:p.Ser1751=
ENST00000374152.6:c.4104C>T	ENSP00000363267.2:p.Ser1368=
ENST00000430799.6:c.1942C>T
ENST00000457599.6:c.4602C>T	ENSP00000387636.2:p.Ser1534=
ENST00000466382.1:c.670C>T
ENST00000532781.1:c.751C>T
NM_006015.4:c.5253C>T , LRG_875t1:c.5253C>T	NP_006006.3:p.Ser1751=
NM_139135.2:c.4602C>T	NP_624361.1:p.Ser1534=
NM_006015.5:c.5253C>T	NP_006006.3:p.Ser1751=
NM_139135.3:c.4602C>T	NP_624361.1:p.Ser1534=
NM_006015.6:c.5253C>T MANE Select	NP_006006.3:p.Ser1751=
NM_139135.4:c.4602C>T	NP_624361.1:p.Ser1534=