Canonical Allele Identifier: CA2695593356

Gene: ARID1A

Linked Data

• dbSNP Id: rs2124137688

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779172del , CM000663.2:g.26779172del	GRCh38
NC_000001.10:g.27105663del , CM000663.1:g.27105663del	GRCh37
NC_000001.9:g.26978250del	NCBI36
NG_029965.1:g.88142del , LRG_875:g.88142del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5274del MANE Select	ENSP00000320485.7:p.Met1759TrpfsTer11
ENST00000374152.7:c.4125del	ENSP00000363267.2:p.Met1376TrpfsTer11
ENST00000430799.7:c.4122del	ENSP00000390317.3:p.Met1375TrpfsTer11
ENST00000466382.2:c.691del
ENST00000636219.1:c.4128del	ENSP00000489842.1:p.Met1377TrpfsTer11
ENST00000637788.1:n.1074del
ENST00000324856.11:c.5274del	ENSP00000320485.7:p.Met1759TrpfsTer11
ENST00000374152.6:c.4125del	ENSP00000363267.2:p.Met1376TrpfsTer11
ENST00000430799.6:c.1963del
ENST00000457599.6:c.4623del	ENSP00000387636.2:p.Met1542TrpfsTer11
ENST00000466382.1:c.691del
ENST00000532781.1:c.772del
NM_006015.4:c.5274del , LRG_875t1:c.5274del	NP_006006.3:p.Met1759TrpfsTer11
NM_139135.2:c.4623del	NP_624361.1:p.Met1542TrpfsTer11
NM_006015.5:c.5274del	NP_006006.3:p.Met1759TrpfsTer11
NM_139135.3:c.4623del	NP_624361.1:p.Met1542TrpfsTer11
NM_006015.6:c.5274del MANE Select	NP_006006.3:p.Met1759TrpfsTer11
NM_139135.4:c.4623del	NP_624361.1:p.Met1542TrpfsTer11