Canonical Allele Identifier: CA1160217999
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26779150G= , CM000663.2:g.26779150G= GRCh38
NC_000001.10:g.27105641G= , CM000663.1:g.27105641G= GRCh37
NC_000001.9:g.26978228G= NCBI36
NG_029965.1:g.88120G= , LRG_875:g.88120G=

Transcript Alleles

HGVS Amino-acid change
ENST00000324856.13:c.5252G= MANE Select ENSP00000320485.7:p.Ser1751=
ENST00000374152.7:c.4103G= ENSP00000363267.2:p.Ser1368=
ENST00000430799.7:c.4100G= ENSP00000390317.3:p.Ser1367=
ENST00000466382.2:c.669G=
ENST00000636219.1:c.4106G= ENSP00000489842.1:p.Ser1369=
ENST00000637788.1:n.1052G=
ENST00000324856.11:c.5252G= ENSP00000320485.7:p.Ser1751=
ENST00000374152.6:c.4103G= ENSP00000363267.2:p.Ser1368=
ENST00000430799.6:c.1941G=
ENST00000457599.6:c.4601G= ENSP00000387636.2:p.Ser1534=
ENST00000466382.1:c.669G=
ENST00000532781.1:c.750G=
NM_006015.4:c.5252G= , LRG_875t1:c.5252G= NP_006006.3:p.Ser1751=
NM_139135.2:c.4601G= NP_624361.1:p.Ser1534=
NM_006015.5:c.5252G= NP_006006.3:p.Ser1751=
NM_139135.3:c.4601G= NP_624361.1:p.Ser1534=
NM_006015.6:c.5252G= MANE Select NP_006006.3:p.Ser1751=
NM_139135.4:c.4601G= NP_624361.1:p.Ser1534=