Canonical Allele Identifier: CA2644294008

Gene: ARID1A

Linked Data

• gnomAD v4: 1-26696421-C-CCCCGCCGCCGCCAGCAGCCTGGGCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696434_26696459dup , CM000663.2:g.26696434_26696459dup	GRCh38
NC_000001.10:g.27022925_27022950dup , CM000663.1:g.27022925_27022950dup	GRCh37
NC_000001.9:g.26895512_26895537dup	NCBI36
NG_029965.1:g.5404_5429dup , LRG_875:g.5404_5429dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.31_56dup MANE Select	ENSP00000320485.7:p.Pro20AlafsTer14
ENST00000430799.7:c.-13+2817_-13+2842dup	ENSP00000390317.3:n.-13+2817_-13+2842dup
ENST00000637465.1:c.-13+334_-13+359dup	ENSP00000490650.1:n.-13+334_-13+359dup
ENST00000324856.11:c.31_56dup	ENSP00000320485.7:p.Pro20AlafsTer14
ENST00000457599.6:c.31_56dup	ENSP00000387636.2:p.Pro20AlafsTer14
NM_006015.4:c.31_56dup , LRG_875t1:c.31_56dup	NP_006006.3:p.Pro20AlafsTer14
NM_139135.2:c.31_56dup	NP_624361.1:p.Pro20AlafsTer14
NM_006015.5:c.31_56dup	NP_006006.3:p.Pro20AlafsTer14
NM_139135.3:c.31_56dup	NP_624361.1:p.Pro20AlafsTer14
NM_006015.6:c.31_56dup MANE Select	NP_006006.3:p.Pro20AlafsTer14
NM_139135.4:c.31_56dup	NP_624361.1:p.Pro20AlafsTer14