Canonical Allele Identifier: CA2644294119
Gene: ARID1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696733dup , CM000663.2:g.26696733dup GRCh38
NC_000001.10:g.27023224dup , CM000663.1:g.27023224dup GRCh37
NC_000001.9:g.26895811dup NCBI36
NG_029965.1:g.5703dup , LRG_875:g.5703dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.330dup MANE Select ENSP00000320485.7:p.Pro111AlafsTer6
ENST00000430799.7:c.-13+3116dup ENSP00000390317.3:n.-13+3116dup
ENST00000637465.1:c.-13+633dup ENSP00000490650.1:n.-13+633dup
ENST00000324856.11:c.330dup ENSP00000320485.7:p.Pro111AlafsTer6
ENST00000457599.6:c.330dup ENSP00000387636.2:p.Pro111AlafsTer6
NM_006015.4:c.330dup , LRG_875t1:c.330dup NP_006006.3:p.Pro111AlafsTer6
NM_139135.2:c.330dup NP_624361.1:p.Pro111AlafsTer6
NM_006015.5:c.330dup NP_006006.3:p.Pro111AlafsTer6
NM_139135.3:c.330dup NP_624361.1:p.Pro111AlafsTer6
NM_006015.6:c.330dup MANE Select NP_006006.3:p.Pro111AlafsTer6
NM_139135.4:c.330dup NP_624361.1:p.Pro111AlafsTer6