Canonical Allele Identifier: CA416989466

Gene: ARID1A

Linked Data

• ClinVar Variation Id: 2981805
• ClinVar RCV Id: RCV003840387
• dbSNP Id: rs2080258847
• gnomAD v4: 1-26696700-C-T
• MyVariant Identifiers: chr1:g.27023191C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696700C>T , CM000663.2:g.26696700C>T	GRCh38
NC_000001.10:g.27023191C>T , CM000663.1:g.27023191C>T	GRCh37
NC_000001.9:g.26895778C>T	NCBI36
NG_029965.1:g.5670C>T , LRG_875:g.5670C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.297C>T MANE Select	ENSP00000320485.7:p.Asp99=
ENST00000430799.7:c.-13+3083C>T	ENSP00000390317.3:n.-13+3083C>T
ENST00000637465.1:c.-13+600C>T	ENSP00000490650.1:n.-13+600C>T
ENST00000324856.11:c.297C>T	ENSP00000320485.7:p.Asp99=
ENST00000457599.6:c.297C>T	ENSP00000387636.2:p.Asp99=
NM_006015.4:c.297C>T , LRG_875t1:c.297C>T	NP_006006.3:p.Asp99=
NM_139135.2:c.297C>T	NP_624361.1:p.Asp99=
NM_006015.5:c.297C>T	NP_006006.3:p.Asp99=
NM_139135.3:c.297C>T	NP_624361.1:p.Asp99=
NM_006015.6:c.297C>T MANE Select	NP_006006.3:p.Asp99=
NM_139135.4:c.297C>T	NP_624361.1:p.Asp99=