Canonical Allele Identifier: CA339265152
Gene: ARID1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2413760
ClinVar RCV Id: RCV003104556
dbSNP Id: rs1392898464
gnomAD v2: 1-27023315-G-A
gnomAD v3: 1-26696824-G-A
gnomAD v4: 1-26696824-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696824G>A , CM000663.2:g.26696824G>A GRCh38
NC_000001.10:g.27023315G>A , CM000663.1:g.27023315G>A GRCh37
NC_000001.9:g.26895902G>A NCBI36
NG_029965.1:g.5794G>A , LRG_875:g.5794G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.421G>A MANE Select ENSP00000320485.7:p.Ala141Thr
ENST00000430799.7:c.-13+3207G>A ENSP00000390317.3:n.-13+3207G>A
ENST00000637465.1:c.-13+724G>A ENSP00000490650.1:n.-13+724G>A
ENST00000324856.11:c.421G>A ENSP00000320485.7:p.Ala141Thr
ENST00000457599.6:c.421G>A ENSP00000387636.2:p.Ala141Thr
NM_006015.4:c.421G>A , LRG_875t1:c.421G>A NP_006006.3:p.Ala141Thr
NM_139135.2:c.421G>A NP_624361.1:p.Ala141Thr
NM_006015.5:c.421G>A NP_006006.3:p.Ala141Thr
NM_139135.3:c.421G>A NP_624361.1:p.Ala141Thr
NM_006015.6:c.421G>A MANE Select NP_006006.3:p.Ala141Thr
NM_139135.4:c.421G>A NP_624361.1:p.Ala141Thr