Canonical Allele Identifier: CA416968242

Gene: ARID1A

Linked Data

• MyVariant Identifiers: chr1:g.27105735T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779244T>C , CM000663.2:g.26779244T>C	GRCh38
NC_000001.10:g.27105735T>C , CM000663.1:g.27105735T>C	GRCh37
NC_000001.9:g.26978322T>C	NCBI36
NG_029965.1:g.88214T>C , LRG_875:g.88214T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5346T>C MANE Select	ENSP00000320485.7:p.Val1782=
ENST00000374152.7:c.4197T>C	ENSP00000363267.2:p.Val1399=
ENST00000430799.7:c.4194T>C	ENSP00000390317.3:p.Val1398=
ENST00000466382.2:c.763T>C
ENST00000636219.1:c.4200T>C	ENSP00000489842.1:p.Val1400=
ENST00000637788.1:n.1146T>C
ENST00000324856.11:c.5346T>C	ENSP00000320485.7:p.Val1782=
ENST00000374152.6:c.4197T>C	ENSP00000363267.2:p.Val1399=
ENST00000430799.6:c.2035T>C
ENST00000457599.6:c.4695T>C	ENSP00000387636.2:p.Val1565=
ENST00000466382.1:c.763T>C
ENST00000532781.1:c.844T>C
NM_006015.4:c.5346T>C , LRG_875t1:c.5346T>C	NP_006006.3:p.Val1782=
NM_139135.2:c.4695T>C	NP_624361.1:p.Val1565=
NM_006015.5:c.5346T>C	NP_006006.3:p.Val1782=
NM_139135.3:c.4695T>C	NP_624361.1:p.Val1565=
NM_006015.6:c.5346T>C MANE Select	NP_006006.3:p.Val1782=
NM_139135.4:c.4695T>C	NP_624361.1:p.Val1565=