Canonical Allele Identifier: CA16617133
Gene: ARID1A HGNC NCBI

Linked Data

ClinVar Variation Id: 422806
ClinVar RCV Id: RCV000478112
dbSNP Id: rs1064796010

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26779160del , CM000663.2:g.26779160del GRCh38
NC_000001.10:g.27105651del , CM000663.1:g.27105651del GRCh37
NC_000001.9:g.26978238del NCBI36
NG_029965.1:g.88130del , LRG_875:g.88130del

Transcript Alleles

HGVS Amino-acid change
ENST00000324856.13:c.5262del MANE Select ENSP00000320485.7:p.Ser1755ValfsTer15
ENST00000374152.7:c.4113del ENSP00000363267.2:p.Ser1372ValfsTer15
ENST00000430799.7:c.4110del ENSP00000390317.3:p.Ser1371ValfsTer15
ENST00000466382.2:c.679del
ENST00000636219.1:c.4116del ENSP00000489842.1:p.Ser1373ValfsTer15
ENST00000637788.1:n.1062del
ENST00000324856.11:c.5262del ENSP00000320485.7:p.Ser1755ValfsTer15
ENST00000374152.6:c.4113del ENSP00000363267.2:p.Ser1372ValfsTer15
ENST00000430799.6:c.1951del
ENST00000457599.6:c.4611del ENSP00000387636.2:p.Ser1538ValfsTer15
ENST00000466382.1:c.679del
ENST00000532781.1:c.760del
NM_006015.4:c.5262del , LRG_875t1:c.5262del NP_006006.3:p.Ser1755ValfsTer15
NM_139135.2:c.4611del NP_624361.1:p.Ser1538ValfsTer15
NM_006015.5:c.5262del NP_006006.3:p.Ser1755ValfsTer15
NM_139135.3:c.4611del NP_624361.1:p.Ser1538ValfsTer15
NM_006015.6:c.5262del MANE Select NP_006006.3:p.Ser1755ValfsTer15
NM_139135.4:c.4611del NP_624361.1:p.Ser1538ValfsTer15