Canonical Allele Identifier: CA339184445

Gene: ARID1A

Linked Data

• dbSNP Id: rs2124137563
• MyVariant Identifiers: chr1:g.27105647T>A (hg19) ; chr1:g.26779156T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779156T>A , CM000663.2:g.26779156T>A	GRCh38
NC_000001.10:g.27105647T>A , CM000663.1:g.27105647T>A	GRCh37
NC_000001.9:g.26978234T>A	NCBI36
NG_029965.1:g.88126T>A , LRG_875:g.88126T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5258T>A MANE Select	ENSP00000320485.7:p.Val1753Glu
ENST00000374152.7:c.4109T>A	ENSP00000363267.2:p.Val1370Glu
ENST00000430799.7:c.4106T>A	ENSP00000390317.3:p.Val1369Glu
ENST00000466382.2:c.675T>A
ENST00000636219.1:c.4112T>A	ENSP00000489842.1:p.Val1371Glu
ENST00000637788.1:n.1058T>A
ENST00000324856.11:c.5258T>A	ENSP00000320485.7:p.Val1753Glu
ENST00000374152.6:c.4109T>A	ENSP00000363267.2:p.Val1370Glu
ENST00000430799.6:c.1947T>A
ENST00000457599.6:c.4607T>A	ENSP00000387636.2:p.Val1536Glu
ENST00000466382.1:c.675T>A
ENST00000532781.1:c.756T>A
NM_006015.4:c.5258T>A , LRG_875t1:c.5258T>A	NP_006006.3:p.Val1753Glu
NM_139135.2:c.4607T>A	NP_624361.1:p.Val1536Glu
NM_006015.5:c.5258T>A	NP_006006.3:p.Val1753Glu
NM_139135.3:c.4607T>A	NP_624361.1:p.Val1536Glu
NM_006015.6:c.5258T>A MANE Select	NP_006006.3:p.Val1753Glu
NM_139135.4:c.4607T>A	NP_624361.1:p.Val1536Glu