Canonical Allele Identifier: CA1160180490
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696334G= , CM000663.2:g.26696334G= GRCh38
NC_000001.10:g.27022825G= , CM000663.1:g.27022825G= GRCh37
NC_000001.9:g.26895412G= NCBI36
NG_029965.1:g.5304G= , LRG_875:g.5304G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.-70G= MANE Select ENSP00000320485.7:n.-70G=
ENST00000430799.7:c.-13+2717G= ENSP00000390317.3:n.-13+2717G=
ENST00000637465.1:c.-13+234G= ENSP00000490650.1:n.-13+234G=
ENST00000324856.11:c.-70G= ENSP00000320485.7:n.-70G=
NM_006015.4:c.-70G= , LRG_875t1:c.-70G= NP_006006.3:n.-70G=
NM_139135.2:c.-70G= NP_624361.1:n.-70G=
XM_011542542.1:c.45+27C= XP_011540844.1:n.45+27C=
NM_006015.5:c.-70G= NP_006006.3:n.-70G=
NM_139135.3:c.-70G= NP_624361.1:n.-70G=
NM_006015.6:c.-70G= MANE Select NP_006006.3:n.-70G=
NM_139135.4:c.-70G= NP_624361.1:n.-70G=