Canonical Allele Identifier: CA1160180496
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696342T= , CM000663.2:g.26696342T= GRCh38
NC_000001.10:g.27022833T= , CM000663.1:g.27022833T= GRCh37
NC_000001.9:g.26895420T= NCBI36
NG_029965.1:g.5312T= , LRG_875:g.5312T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.-62T= MANE Select ENSP00000320485.7:n.-62T=
ENST00000430799.7:c.-13+2725T= ENSP00000390317.3:n.-13+2725T=
ENST00000637465.1:c.-13+242T= ENSP00000490650.1:n.-13+242T=
ENST00000324856.11:c.-62T= ENSP00000320485.7:n.-62T=
NM_006015.4:c.-62T= , LRG_875t1:c.-62T= NP_006006.3:n.-62T=
NM_139135.2:c.-62T= NP_624361.1:n.-62T=
XM_011542542.1:c.45+19A= XP_011540844.1:n.45+19A=
NM_006015.5:c.-62T= NP_006006.3:n.-62T=
NM_139135.3:c.-62T= NP_624361.1:n.-62T=
NM_006015.6:c.-62T= MANE Select NP_006006.3:n.-62T=
NM_139135.4:c.-62T= NP_624361.1:n.-62T=