Canonical Allele Identifier: CA339184921

Gene: ARID1A

Linked Data

• dbSNP Id: rs2124138465
• MyVariant Identifiers: chr1:g.27105742G>T (hg19) ; chr1:g.26779251G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779251G>T , CM000663.2:g.26779251G>T	GRCh38
NC_000001.10:g.27105742G>T , CM000663.1:g.27105742G>T	GRCh37
NC_000001.9:g.26978329G>T	NCBI36
NG_029965.1:g.88221G>T , LRG_875:g.88221G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5353G>T MANE Select	ENSP00000320485.7:p.Asp1785Tyr
ENST00000374152.7:c.4204G>T	ENSP00000363267.2:p.Asp1402Tyr
ENST00000430799.7:c.4201G>T	ENSP00000390317.3:p.Asp1401Tyr
ENST00000466382.2:c.770G>T
ENST00000636219.1:c.4207G>T	ENSP00000489842.1:p.Asp1403Tyr
ENST00000637788.1:n.1153G>T
ENST00000324856.11:c.5353G>T	ENSP00000320485.7:p.Asp1785Tyr
ENST00000374152.6:c.4204G>T	ENSP00000363267.2:p.Asp1402Tyr
ENST00000430799.6:c.2042G>T
ENST00000457599.6:c.4702G>T	ENSP00000387636.2:p.Asp1568Tyr
ENST00000466382.1:c.770G>T
ENST00000532781.1:c.851G>T
NM_006015.4:c.5353G>T , LRG_875t1:c.5353G>T	NP_006006.3:p.Asp1785Tyr
NM_139135.2:c.4702G>T	NP_624361.1:p.Asp1568Tyr
NM_006015.5:c.5353G>T	NP_006006.3:p.Asp1785Tyr
NM_139135.3:c.4702G>T	NP_624361.1:p.Asp1568Tyr
NM_006015.6:c.5353G>T MANE Select	NP_006006.3:p.Asp1785Tyr
NM_139135.4:c.4702G>T	NP_624361.1:p.Asp1568Tyr