Canonical Allele Identifier: CA1160218006

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779159_26779160delinsCT , CM000663.2:g.26779159_26779160delinsCT	GRCh38
NC_000001.10:g.27105650_27105651delinsCT , CM000663.1:g.27105650_27105651delinsCT	GRCh37
NC_000001.9:g.26978237_26978238delinsCT	NCBI36
NG_029965.1:g.88129_88130delinsCT , LRG_875:g.88129_88130delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5261_5262delinsCT MANE Select	ENSP00000320485.7:p.Ser1754=
ENST00000374152.7:c.4112_4113delinsCT	ENSP00000363267.2:p.Ser1371=
ENST00000430799.7:c.4109_4110delinsCT	ENSP00000390317.3:p.Ser1370=
ENST00000466382.2:c.678_679delinsCT
ENST00000636219.1:c.4115_4116delinsCT	ENSP00000489842.1:p.Ser1372=
ENST00000637788.1:n.1061_1062delinsCT
ENST00000324856.11:c.5261_5262delinsCT	ENSP00000320485.7:p.Ser1754=
ENST00000374152.6:c.4112_4113delinsCT	ENSP00000363267.2:p.Ser1371=
ENST00000430799.6:c.1950_1951delinsCT
ENST00000457599.6:c.4610_4611delinsCT	ENSP00000387636.2:p.Ser1537=
ENST00000466382.1:c.678_679delinsCT
ENST00000532781.1:c.759_760delinsCT
NM_006015.4:c.5261_5262delinsCT , LRG_875t1:c.5261_5262delinsCT	NP_006006.3:p.Ser1754=
NM_139135.2:c.4610_4611delinsCT	NP_624361.1:p.Ser1537=
NM_006015.5:c.5261_5262delinsCT	NP_006006.3:p.Ser1754=
NM_139135.3:c.4610_4611delinsCT	NP_624361.1:p.Ser1537=
NM_006015.6:c.5261_5262delinsCT MANE Select	NP_006006.3:p.Ser1754=
NM_139135.4:c.4610_4611delinsCT	NP_624361.1:p.Ser1537=