Canonical Allele Identifier: CA2573332525
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26779197_26779198insCTT , CM000663.2:g.26779197_26779198insCTT GRCh38
NC_000001.10:g.27105688_27105689insCTT , CM000663.1:g.27105688_27105689insCTT GRCh37
NC_000001.9:g.26978275_26978276insCTT NCBI36
NG_029965.1:g.88167_88168insCTT , LRG_875:g.88167_88168insCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.5299_5300insCTT MANE Select ENSP00000320485.7:p.Glu1767AlafsTer2
ENST00000374152.7:c.4150_4151insCTT ENSP00000363267.2:p.Glu1384AlafsTer2
ENST00000430799.7:c.4147_4148insCTT ENSP00000390317.3:p.Glu1383AlafsTer2
ENST00000466382.2:c.716_717insCTT
ENST00000636219.1:c.4153_4154insCTT ENSP00000489842.1:p.Glu1385AlafsTer2
ENST00000637788.1:n.1099_1100insCTT
ENST00000324856.11:c.5299_5300insCTT ENSP00000320485.7:p.Glu1767AlafsTer2
ENST00000374152.6:c.4150_4151insCTT ENSP00000363267.2:p.Glu1384AlafsTer2
ENST00000430799.6:c.1988_1989insCTT
ENST00000457599.6:c.4648_4649insCTT ENSP00000387636.2:p.Glu1550AlafsTer2
ENST00000466382.1:c.716_717insCTT
ENST00000532781.1:c.797_798insCTT
NM_006015.4:c.5299_5300insCTT , LRG_875t1:c.5299_5300insCTT NP_006006.3:p.Glu1767AlafsTer2
NM_139135.2:c.4648_4649insCTT NP_624361.1:p.Glu1550AlafsTer2
NM_006015.5:c.5299_5300insCTT NP_006006.3:p.Glu1767AlafsTer2
NM_139135.3:c.4648_4649insCTT NP_624361.1:p.Glu1550AlafsTer2
NM_006015.6:c.5299_5300insCTT MANE Select NP_006006.3:p.Glu1767AlafsTer2
NM_139135.4:c.4648_4649insCTT NP_624361.1:p.Glu1550AlafsTer2