Canonical Allele Identifier: CA2644294015

Gene: ARID1A

Linked Data

• gnomAD v4: 1-26696431-GCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696432_26696434del , CM000663.2:g.26696432_26696434del	GRCh38
NC_000001.10:g.27022923_27022925del , CM000663.1:g.27022923_27022925del	GRCh37
NC_000001.9:g.26895510_26895512del	NCBI36
NG_029965.1:g.5402_5404del , LRG_875:g.5402_5404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.29_31del MANE Select	ENSP00000320485.7:p.Ala10_Ser11delinsGly
ENST00000430799.7:c.-13+2815_-13+2817del	ENSP00000390317.3:n.-13+2815_-13+2817del
ENST00000637465.1:c.-13+332_-13+334del	ENSP00000490650.1:n.-13+332_-13+334del
ENST00000324856.11:c.29_31del	ENSP00000320485.7:p.Ala10_Ser11delinsGly
ENST00000457599.6:c.29_31del	ENSP00000387636.2:p.Ala10_Ser11delinsGly
NM_006015.4:c.29_31del , LRG_875t1:c.29_31del	NP_006006.3:p.Ala10_Ser11delinsGly
NM_139135.2:c.29_31del	NP_624361.1:p.Ala10_Ser11delinsGly
NM_006015.5:c.29_31del	NP_006006.3:p.Ala10_Ser11delinsGly
NM_139135.3:c.29_31del	NP_624361.1:p.Ala10_Ser11delinsGly
NM_006015.6:c.29_31del MANE Select	NP_006006.3:p.Ala10_Ser11delinsGly
NM_139135.4:c.29_31del	NP_624361.1:p.Ala10_Ser11delinsGly