Canonical Allele Identifier: CA1160180802

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696793_26696794delinsTG , CM000663.2:g.26696793_26696794delinsTG	GRCh38
NC_000001.10:g.27023284_27023285delinsTG , CM000663.1:g.27023284_27023285delinsTG	GRCh37
NC_000001.9:g.26895871_26895872delinsTG	NCBI36
NG_029965.1:g.5763_5764delinsTG , LRG_875:g.5763_5764delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.390_391delinsTG MANE Select	ENSP00000320485.7:p.Asp130=
ENST00000430799.7:c.-13+3176_-13+3177delinsTG	ENSP00000390317.3:n.-13+3176_-13+3177delinsTG
ENST00000637465.1:c.-13+693_-13+694delinsTG	ENSP00000490650.1:n.-13+693_-13+694delinsTG
ENST00000324856.11:c.390_391delinsTG	ENSP00000320485.7:p.Asp130=
ENST00000457599.6:c.390_391delinsTG	ENSP00000387636.2:p.Asp130=
NM_006015.4:c.390_391delinsTG , LRG_875t1:c.390_391delinsTG	NP_006006.3:p.Asp130=
NM_139135.2:c.390_391delinsTG	NP_624361.1:p.Asp130=
NM_006015.5:c.390_391delinsTG	NP_006006.3:p.Asp130=
NM_139135.3:c.390_391delinsTG	NP_624361.1:p.Asp130=
NM_006015.6:c.390_391delinsTG MANE Select	NP_006006.3:p.Asp130=
NM_139135.4:c.390_391delinsTG	NP_624361.1:p.Asp130=