Canonical Allele Identifier: CA339264935
Gene: ARID1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696753T>G , CM000663.2:g.26696753T>G GRCh38
NC_000001.10:g.27023244T>G , CM000663.1:g.27023244T>G GRCh37
NC_000001.9:g.26895831T>G NCBI36
NG_029965.1:g.5723T>G , LRG_875:g.5723T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.350T>G MANE Select ENSP00000320485.7:p.Leu117Arg
ENST00000430799.7:c.-13+3136T>G ENSP00000390317.3:n.-13+3136T>G
ENST00000637465.1:c.-13+653T>G ENSP00000490650.1:n.-13+653T>G
ENST00000324856.11:c.350T>G ENSP00000320485.7:p.Leu117Arg
ENST00000457599.6:c.350T>G ENSP00000387636.2:p.Leu117Arg
NM_006015.4:c.350T>G , LRG_875t1:c.350T>G NP_006006.3:p.Leu117Arg
NM_139135.2:c.350T>G NP_624361.1:p.Leu117Arg
NM_006015.5:c.350T>G NP_006006.3:p.Leu117Arg
NM_139135.3:c.350T>G NP_624361.1:p.Leu117Arg
NM_006015.6:c.350T>G MANE Select NP_006006.3:p.Leu117Arg
NM_139135.4:c.350T>G NP_624361.1:p.Leu117Arg