Canonical Allele Identifier: CA1160180688
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696632G= , CM000663.2:g.26696632G= GRCh38
NC_000001.10:g.27023123G= , CM000663.1:g.27023123G= GRCh37
NC_000001.9:g.26895710G= NCBI36
NG_029965.1:g.5602G= , LRG_875:g.5602G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.229G= MANE Select ENSP00000320485.7:p.Ala77=
ENST00000430799.7:c.-13+3015G= ENSP00000390317.3:n.-13+3015G=
ENST00000637465.1:c.-13+532G= ENSP00000490650.1:n.-13+532G=
ENST00000324856.11:c.229G= ENSP00000320485.7:p.Ala77=
ENST00000457599.6:c.229G= ENSP00000387636.2:p.Ala77=
NM_006015.4:c.229G= , LRG_875t1:c.229G= NP_006006.3:p.Ala77=
NM_139135.2:c.229G= NP_624361.1:p.Ala77=
NM_006015.5:c.229G= NP_006006.3:p.Ala77=
NM_139135.3:c.229G= NP_624361.1:p.Ala77=
NM_006015.6:c.229G= MANE Select NP_006006.3:p.Ala77=
NM_139135.4:c.229G= NP_624361.1:p.Ala77=