Canonical Allele Identifier: CA1160218036
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26779217A= , CM000663.2:g.26779217A= GRCh38
NC_000001.10:g.27105708A= , CM000663.1:g.27105708A= GRCh37
NC_000001.9:g.26978295A= NCBI36
NG_029965.1:g.88187A= , LRG_875:g.88187A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.5319A= MANE Select ENSP00000320485.7:p.Leu1773=
ENST00000374152.7:c.4170A= ENSP00000363267.2:p.Leu1390=
ENST00000430799.7:c.4167A= ENSP00000390317.3:p.Leu1389=
ENST00000466382.2:c.736A=
ENST00000636219.1:c.4173A= ENSP00000489842.1:p.Leu1391=
ENST00000637788.1:n.1119A=
ENST00000324856.11:c.5319A= ENSP00000320485.7:p.Leu1773=
ENST00000374152.6:c.4170A= ENSP00000363267.2:p.Leu1390=
ENST00000430799.6:c.2008A=
ENST00000457599.6:c.4668A= ENSP00000387636.2:p.Leu1556=
ENST00000466382.1:c.736A=
ENST00000532781.1:c.817A=
NM_006015.4:c.5319A= , LRG_875t1:c.5319A= NP_006006.3:p.Leu1773=
NM_139135.2:c.4668A= NP_624361.1:p.Leu1556=
NM_006015.5:c.5319A= NP_006006.3:p.Leu1773=
NM_139135.3:c.4668A= NP_624361.1:p.Leu1556=
NM_006015.6:c.5319A= MANE Select NP_006006.3:p.Leu1773=
NM_139135.4:c.4668A= NP_624361.1:p.Leu1556=