Canonical Allele Identifier: CA1160218028

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779201T= , CM000663.2:g.26779201T=	GRCh38
NC_000001.10:g.27105692T= , CM000663.1:g.27105692T=	GRCh37
NC_000001.9:g.26978279T=	NCBI36
NG_029965.1:g.88171T= , LRG_875:g.88171T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5303T= MANE Select	ENSP00000320485.7:p.Leu1768=
ENST00000374152.7:c.4154T=	ENSP00000363267.2:p.Leu1385=
ENST00000430799.7:c.4151T=	ENSP00000390317.3:p.Leu1384=
ENST00000466382.2:c.720T=
ENST00000636219.1:c.4157T=	ENSP00000489842.1:p.Leu1386=
ENST00000637788.1:n.1103T=
ENST00000324856.11:c.5303T=	ENSP00000320485.7:p.Leu1768=
ENST00000374152.6:c.4154T=	ENSP00000363267.2:p.Leu1385=
ENST00000430799.6:c.1992T=
ENST00000457599.6:c.4652T=	ENSP00000387636.2:p.Leu1551=
ENST00000466382.1:c.720T=
ENST00000532781.1:c.801T=
NM_006015.4:c.5303T= , LRG_875t1:c.5303T=	NP_006006.3:p.Leu1768=
NM_139135.2:c.4652T=	NP_624361.1:p.Leu1551=
NM_006015.5:c.5303T=	NP_006006.3:p.Leu1768=
NM_139135.3:c.4652T=	NP_624361.1:p.Leu1551=
NM_006015.6:c.5303T= MANE Select	NP_006006.3:p.Leu1768=
NM_139135.4:c.4652T=	NP_624361.1:p.Leu1551=