Canonical Allele Identifier: CA1160197018

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26731100C= , CM000663.2:g.26731100C=	GRCh38
NC_000001.10:g.27057591C= , CM000663.1:g.27057591C=	GRCh37
NC_000001.9:g.26930178C=	NCBI36
NG_029965.1:g.40070C= , LRG_875:g.40070C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.1351-52C= MANE Select	ENSP00000320485.7:n.1351-52C=
ENST00000374152.7:c.202-52C=	ENSP00000363267.2:n.202-52C=
ENST00000430799.7:c.202-52C=	ENSP00000390317.3:n.202-52C=
ENST00000636219.1:c.208-52C=	ENSP00000489842.1:n.208-52C=
ENST00000637465.1:c.202-52C=	ENSP00000490650.1:n.202-52C=
ENST00000324856.11:c.1351-52C=	ENSP00000320485.7:n.1351-52C=
ENST00000374152.6:c.202-52C=	ENSP00000363267.2:n.202-52C=
ENST00000457599.6:c.1351-52C=	ENSP00000387636.2:n.1351-52C=
ENST00000524572.1:c.202-52C=	ENSP00000432473.1:n.202-52C=
ENST00000615191.4:c.202-52C=	ENSP00000478955.1:n.202-52C=
NM_006015.4:c.1351-52C= , LRG_875t1:c.1351-52C=	NP_006006.3:n.1351-52C=
NM_139135.2:c.1351-52C=	NP_624361.1:n.1351-52C=
NM_006015.5:c.1351-52C=	NP_006006.3:n.1351-52C=
NM_139135.3:c.1351-52C=	NP_624361.1:n.1351-52C=
NM_006015.6:c.1351-52C= MANE Select	NP_006006.3:n.1351-52C=
NM_139135.4:c.1351-52C=	NP_624361.1:n.1351-52C=