Canonical Allele Identifier: CA521909931

Gene: ARID1A

Linked Data

• dbSNP Id: rs1172366554
• gnomAD v2: 1-27022976-GAGC-G
• gnomAD v4: 1-26696485-GAGC-G
• MyVariant Identifiers: chr1:g.27022977_27022979del (hg19) ; chr1:g.26696486_26696488del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696495_26696497del , CM000663.2:g.26696495_26696497del	GRCh38
NC_000001.10:g.27022986_27022988del , CM000663.1:g.27022986_27022988del	GRCh37
NC_000001.9:g.26895573_26895575del	NCBI36
NG_029965.1:g.5465_5467del , LRG_875:g.5465_5467del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.92_94del MANE Select	ENSP00000320485.7:p.Gln31del
ENST00000430799.7:c.-13+2878_-13+2880del	ENSP00000390317.3:n.-13+2878_-13+2880del
ENST00000637465.1:c.-13+395_-13+397del	ENSP00000490650.1:n.-13+395_-13+397del
ENST00000324856.11:c.92_94del	ENSP00000320485.7:p.Gln31del
ENST00000457599.6:c.92_94del	ENSP00000387636.2:p.Gln31del
NM_006015.4:c.92_94del , LRG_875t1:c.92_94del	NP_006006.3:p.Gln31del
NM_139135.2:c.92_94del	NP_624361.1:p.Gln31del
NM_006015.5:c.92_94del	NP_006006.3:p.Gln31del
NM_139135.3:c.92_94del	NP_624361.1:p.Gln31del
NM_006015.6:c.92_94del MANE Select	NP_006006.3:p.Gln31del
NM_139135.4:c.92_94del	NP_624361.1:p.Gln31del