Canonical Allele Identifier: CA339184908

Gene: ARID1A

Linked Data

• dbSNP Id: rs2124138433
• MyVariant Identifiers: chr1:g.27105739A>T (hg19) ; chr1:g.26779248A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5350A>T MANE Select	ENSP00000320485.7:p.Asn1784Tyr
ENST00000374152.7:c.4201A>T	ENSP00000363267.2:p.Asn1401Tyr
ENST00000430799.7:c.4198A>T	ENSP00000390317.3:p.Asn1400Tyr
ENST00000466382.2:c.767A>T
ENST00000636219.1:c.4204A>T	ENSP00000489842.1:p.Asn1402Tyr
ENST00000637788.1:n.1150A>T
ENST00000324856.11:c.5350A>T	ENSP00000320485.7:p.Asn1784Tyr
ENST00000374152.6:c.4201A>T	ENSP00000363267.2:p.Asn1401Tyr
ENST00000430799.6:c.2039A>T
ENST00000457599.6:c.4699A>T	ENSP00000387636.2:p.Asn1567Tyr
ENST00000466382.1:c.767A>T
ENST00000532781.1:c.848A>T
NM_006015.4:c.5350A>T , LRG_875t1:c.5350A>T	NP_006006.3:p.Asn1784Tyr
NM_139135.2:c.4699A>T	NP_624361.1:p.Asn1567Tyr
NM_006015.5:c.5350A>T	NP_006006.3:p.Asn1784Tyr
NM_139135.3:c.4699A>T	NP_624361.1:p.Asn1567Tyr
NM_006015.6:c.5350A>T MANE Select	NP_006006.3:p.Asn1784Tyr
NM_139135.4:c.4699A>T	NP_624361.1:p.Asn1567Tyr