Canonical Allele Identifier: CA339184907

Gene: ARID1A

Linked Data

• MyVariant Identifiers: chr1:g.27105739A>G (hg19) ; chr1:g.26779248A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779248A>G , CM000663.2:g.26779248A>G	GRCh38
NC_000001.10:g.27105739A>G , CM000663.1:g.27105739A>G	GRCh37
NC_000001.9:g.26978326A>G	NCBI36
NG_029965.1:g.88218A>G , LRG_875:g.88218A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5350A>G MANE Select	ENSP00000320485.7:p.Asn1784Asp
ENST00000374152.7:c.4201A>G	ENSP00000363267.2:p.Asn1401Asp
ENST00000430799.7:c.4198A>G	ENSP00000390317.3:p.Asn1400Asp
ENST00000466382.2:c.767A>G
ENST00000636219.1:c.4204A>G	ENSP00000489842.1:p.Asn1402Asp
ENST00000637788.1:n.1150A>G
ENST00000324856.11:c.5350A>G	ENSP00000320485.7:p.Asn1784Asp
ENST00000374152.6:c.4201A>G	ENSP00000363267.2:p.Asn1401Asp
ENST00000430799.6:c.2039A>G
ENST00000457599.6:c.4699A>G	ENSP00000387636.2:p.Asn1567Asp
ENST00000466382.1:c.767A>G
ENST00000532781.1:c.848A>G
NM_006015.4:c.5350A>G , LRG_875t1:c.5350A>G	NP_006006.3:p.Asn1784Asp
NM_139135.2:c.4699A>G	NP_624361.1:p.Asn1567Asp
NM_006015.5:c.5350A>G	NP_006006.3:p.Asn1784Asp
NM_139135.3:c.4699A>G	NP_624361.1:p.Asn1567Asp
NM_006015.6:c.5350A>G MANE Select	NP_006006.3:p.Asn1784Asp
NM_139135.4:c.4699A>G	NP_624361.1:p.Asn1567Asp