Canonical Allele Identifier: CA2644294079

Gene: ARID1A

Linked Data

• gnomAD v4: 1-26696659-GGCGGAGCCGGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696664_26696675del , CM000663.2:g.26696664_26696675del	GRCh38
NC_000001.10:g.27023155_27023166del , CM000663.1:g.27023155_27023166del	GRCh37
NC_000001.9:g.26895742_26895753del	NCBI36
NG_029965.1:g.5634_5645del , LRG_875:g.5634_5645del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.261_272del MANE Select	ENSP00000320485.7:p.Ala88_Gly91del
ENST00000430799.7:c.-13+3047_-13+3058del	ENSP00000390317.3:n.-13+3047_-13+3058del
ENST00000637465.1:c.-13+564_-13+575del	ENSP00000490650.1:n.-13+564_-13+575del
ENST00000324856.11:c.261_272del	ENSP00000320485.7:p.Ala88_Gly91del
ENST00000457599.6:c.261_272del	ENSP00000387636.2:p.Ala88_Gly91del
NM_006015.4:c.261_272del , LRG_875t1:c.261_272del	NP_006006.3:p.Ala88_Gly91del
NM_139135.2:c.261_272del	NP_624361.1:p.Ala88_Gly91del
NM_006015.5:c.261_272del	NP_006006.3:p.Ala88_Gly91del
NM_139135.3:c.261_272del	NP_624361.1:p.Ala88_Gly91del
NM_006015.6:c.261_272del MANE Select	NP_006006.3:p.Ala88_Gly91del
NM_139135.4:c.261_272del	NP_624361.1:p.Ala88_Gly91del