Canonical Allele Identifier: CA339172557
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26773899G>T , CM000663.2:g.26773899G>T GRCh38
NC_000001.10:g.27100390G>T , CM000663.1:g.27100390G>T GRCh37
NC_000001.9:g.26972977G>T NCBI36
NG_029965.1:g.82869G>T , LRG_875:g.82869G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.4101+1G>T MANE Select ENSP00000320485.7:n.4101+1G>T
ENST00000374152.7:c.2952+1G>T ENSP00000363267.2:n.2952+1G>T
ENST00000430799.7:c.2949+1G>T ENSP00000390317.3:n.2949+1G>T
ENST00000466382.2:c.410+1G>T
ENST00000636072.1:n.494+1G>T
ENST00000636219.1:c.2955+1G>T ENSP00000489842.1:n.2955+1G>T
ENST00000636794.1:n.407+1G>T
ENST00000324856.11:c.4101+1G>T ENSP00000320485.7:n.4101+1G>T
ENST00000374152.6:c.2952+1G>T ENSP00000363267.2:n.2952+1G>T
ENST00000430799.6:c.790+1G>T
ENST00000457599.6:c.4101+1G>T ENSP00000387636.2:n.4101+1G>T
ENST00000466382.1:c.410+1G>T
ENST00000615191.4:c.2949+1G>T ENSP00000478955.1:n.2949+1G>T
NM_006015.4:c.4101+1G>T , LRG_875t1:c.4101+1G>T NP_006006.3:n.4101+1G>T
NM_139135.2:c.4101+1G>T NP_624361.1:n.4101+1G>T
NM_006015.5:c.4101+1G>T NP_006006.3:n.4101+1G>T
NM_139135.3:c.4101+1G>T NP_624361.1:n.4101+1G>T
NM_006015.6:c.4101+1G>T MANE Select NP_006006.3:n.4101+1G>T
NM_139135.4:c.4101+1G>T NP_624361.1:n.4101+1G>T