Canonical Allele Identifier: CA707671

Gene: ARID1A

Linked Data

• ClinVar Variation Id: 1981194
• ClinVar RCV Id: RCV002751328
• dbSNP Id: rs757247033
• ExAC: 1:27105707 TAGAAGAGGAAGA / T
• gnomAD v2: 1-27105707-TAGAAGAGGAAGA-T
• gnomAD v4: 1-26779216-TAGAAGAGGAAGA-T
• MyVariant Identifiers: chr1:g.27105708_27105719del (hg19) ; chr1:g.26779217_26779228del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779228_26779239del , CM000663.2:g.26779228_26779239del	GRCh38
NC_000001.10:g.27105719_27105730del , CM000663.1:g.27105719_27105730del	GRCh37
NC_000001.9:g.26978306_26978317del	NCBI36
NG_029965.1:g.88198_88209del , LRG_875:g.88198_88209del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5330_5341del MANE Select	ENSP00000320485.7:p.Glu1777_Glu1780del
ENST00000374152.7:c.4181_4192del	ENSP00000363267.2:p.Glu1394_Glu1397del
ENST00000430799.7:c.4178_4189del	ENSP00000390317.3:p.Glu1393_Glu1396del
ENST00000466382.2:c.747_758del
ENST00000636219.1:c.4184_4195del	ENSP00000489842.1:p.Glu1395_Glu1398del
ENST00000637788.1:n.1130_1141del
ENST00000324856.11:c.5330_5341del	ENSP00000320485.7:p.Glu1777_Glu1780del
ENST00000374152.6:c.4181_4192del	ENSP00000363267.2:p.Glu1394_Glu1397del
ENST00000430799.6:c.2019_2030del
ENST00000457599.6:c.4679_4690del	ENSP00000387636.2:p.Glu1560_Glu1563del
ENST00000466382.1:c.747_758del
ENST00000532781.1:c.828_839del
NM_006015.4:c.5330_5341del , LRG_875t1:c.5330_5341del	NP_006006.3:p.Glu1777_Glu1780del
NM_139135.2:c.4679_4690del	NP_624361.1:p.Glu1560_Glu1563del
NM_006015.5:c.5330_5341del	NP_006006.3:p.Glu1777_Glu1780del
NM_139135.3:c.4679_4690del	NP_624361.1:p.Glu1560_Glu1563del
NM_006015.6:c.5330_5341del MANE Select	NP_006006.3:p.Glu1777_Glu1780del
NM_139135.4:c.4679_4690del	NP_624361.1:p.Glu1560_Glu1563del