Canonical Allele Identifier: CA734489716

Gene: ARID1A

Linked Data

• dbSNP Id: rs1421881390
• gnomAD v3: 1-26696397-G-A
• gnomAD v4: 1-26696397-G-A
• MyVariant Identifiers: chr1:g.27022888G>A (hg19) ; chr1:g.26696397G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696397G>A , CM000663.2:g.26696397G>A	GRCh38
NC_000001.10:g.27022888G>A , CM000663.1:g.27022888G>A	GRCh37
NC_000001.9:g.26895475G>A	NCBI36
NG_029965.1:g.5367G>A , LRG_875:g.5367G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.-7G>A MANE Select	ENSP00000320485.7:n.-7G>A
ENST00000430799.7:c.-13+2780G>A	ENSP00000390317.3:n.-13+2780G>A
ENST00000637465.1:c.-13+297G>A	ENSP00000490650.1:n.-13+297G>A
ENST00000324856.11:c.-7G>A	ENSP00000320485.7:n.-7G>A
NM_006015.4:c.-7G>A , LRG_875t1:c.-7G>A	NP_006006.3:n.-7G>A
NM_139135.2:c.-7G>A	NP_624361.1:n.-7G>A
XM_011542542.1:c.9C>T	XP_011540844.1:p.Pro3=
NM_006015.5:c.-7G>A	NP_006006.3:n.-7G>A
NM_139135.3:c.-7G>A	NP_624361.1:n.-7G>A
NM_006015.6:c.-7G>A MANE Select	NP_006006.3:n.-7G>A
NM_139135.4:c.-7G>A	NP_624361.1:n.-7G>A