Canonical Allele Identifier: CA1160194593
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs11247593

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26725589G>T , CM000663.2:g.26725589G>T GRCh38
NC_000001.10:g.27052080G>T , CM000663.1:g.27052080G>T GRCh37
NC_000001.9:g.26924667G>T NCBI36
NG_029965.1:g.34559G>T , LRG_875:g.34559G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000324856.13:c.1138-4062G>T MANE Select ENSP00000320485.7:n.1138-4062G>T
ENST00000430799.7:c.-12-4062G>T ENSP00000390317.3:n.-12-4062G>T
ENST00000637465.1:c.-12-4062G>T ENSP00000490650.1:n.-12-4062G>T
ENST00000324856.11:c.1138-4062G>T ENSP00000320485.7:n.1138-4062G>T
ENST00000457599.6:c.1138-4062G>T ENSP00000387636.2:n.1138-4062G>T
NM_006015.4:c.1138-4062G>T , LRG_875t1:c.1138-4062G>T NP_006006.3:n.1138-4062G>T
NM_139135.2:c.1138-4062G>T NP_624361.1:n.1138-4062G>T
NM_006015.5:c.1138-4062G>T NP_006006.3:n.1138-4062G>T
NM_139135.3:c.1138-4062G>T NP_624361.1:n.1138-4062G>T
NM_006015.6:c.1138-4062G>T MANE Select NP_006006.3:n.1138-4062G>T
NM_139135.4:c.1138-4062G>T NP_624361.1:n.1138-4062G>T