Canonical Allele Identifier: CA339267990

Gene: ARID1A

Linked Data

• dbSNP Id: rs2124788072
• MyVariant Identifiers: chr1:g.27057697C>A (hg19) ; chr1:g.26731206C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26731206C>A , CM000663.2:g.26731206C>A	GRCh38
NC_000001.10:g.27057697C>A , CM000663.1:g.27057697C>A	GRCh37
NC_000001.9:g.26930284C>A	NCBI36
NG_029965.1:g.40176C>A , LRG_875:g.40176C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.1405C>A MANE Select	ENSP00000320485.7:p.Pro469Thr
ENST00000374152.7:c.256C>A	ENSP00000363267.2:p.Pro86Thr
ENST00000430799.7:c.256C>A	ENSP00000390317.3:p.Pro86Thr
ENST00000636219.1:c.262C>A	ENSP00000489842.1:p.Pro88Thr
ENST00000637465.1:c.256C>A	ENSP00000490650.1:p.Pro86Thr
ENST00000324856.11:c.1405C>A	ENSP00000320485.7:p.Pro469Thr
ENST00000374152.6:c.256C>A	ENSP00000363267.2:p.Pro86Thr
ENST00000457599.6:c.1405C>A	ENSP00000387636.2:p.Pro469Thr
ENST00000524572.1:c.256C>A	ENSP00000432473.1:p.Pro86Thr
ENST00000615191.4:c.256C>A	ENSP00000478955.1:p.Pro86Thr
NM_006015.4:c.1405C>A , LRG_875t1:c.1405C>A	NP_006006.3:p.Pro469Thr
NM_139135.2:c.1405C>A	NP_624361.1:p.Pro469Thr
NM_006015.5:c.1405C>A	NP_006006.3:p.Pro469Thr
NM_139135.3:c.1405C>A	NP_624361.1:p.Pro469Thr
NM_006015.6:c.1405C>A MANE Select	NP_006006.3:p.Pro469Thr
NM_139135.4:c.1405C>A	NP_624361.1:p.Pro469Thr