Canonical Allele Identifier: CA706579
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs767811400
gnomAD v2: 1-27023180-G-A
gnomAD v4: 1-26696689-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696689G>A , CM000663.2:g.26696689G>A GRCh38
NC_000001.10:g.27023180G>A , CM000663.1:g.27023180G>A GRCh37
NC_000001.9:g.26895767G>A NCBI36
NG_029965.1:g.5659G>A , LRG_875:g.5659G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.286G>A MANE Select ENSP00000320485.7:p.Ala96Thr
ENST00000430799.7:c.-13+3072G>A ENSP00000390317.3:n.-13+3072G>A
ENST00000637465.1:c.-13+589G>A ENSP00000490650.1:n.-13+589G>A
ENST00000324856.11:c.286G>A ENSP00000320485.7:p.Ala96Thr
ENST00000457599.6:c.286G>A ENSP00000387636.2:p.Ala96Thr
NM_006015.4:c.286G>A , LRG_875t1:c.286G>A NP_006006.3:p.Ala96Thr
NM_139135.2:c.286G>A NP_624361.1:p.Ala96Thr
NM_006015.5:c.286G>A NP_006006.3:p.Ala96Thr
NM_139135.3:c.286G>A NP_624361.1:p.Ala96Thr
NM_006015.6:c.286G>A MANE Select NP_006006.3:p.Ala96Thr
NM_139135.4:c.286G>A NP_624361.1:p.Ala96Thr