Canonical Allele Identifier: CA1160211817
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs2081106201

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26773711_26773716dup , CM000663.2:g.26773711_26773716dup GRCh38
NC_000001.10:g.27100202_27100207dup , CM000663.1:g.27100202_27100207dup GRCh37
NC_000001.9:g.26972789_26972794dup NCBI36
NG_029965.1:g.82681_82686dup , LRG_875:g.82681_82686dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.3998_4003dup MANE Select ENSP00000320485.7:p.Gln1334_Arg1335insGlnGln
ENST00000374152.7:c.2849_2854dup ENSP00000363267.2:p.Gln951_Arg952insGlnGln
ENST00000430799.7:c.2846_2851dup ENSP00000390317.3:p.Gln950_Arg951insGlnGln
ENST00000466382.2:c.307_312dup
ENST00000636072.1:n.391_396dup
ENST00000636219.1:c.2852_2857dup ENSP00000489842.1:p.Gln952_Arg953insGlnGln
ENST00000636794.1:n.304_309dup
ENST00000324856.11:c.3998_4003dup ENSP00000320485.7:p.Gln1334_Arg1335insGlnGln
ENST00000374152.6:c.2849_2854dup ENSP00000363267.2:p.Gln951_Arg952insGlnGln
ENST00000430799.6:c.687_692dup
ENST00000457599.6:c.3998_4003dup ENSP00000387636.2:p.Gln1334_Arg1335insGlnGln
ENST00000466382.1:c.307_312dup
ENST00000615191.4:c.2846_2851dup ENSP00000478955.1:p.Gln950_Arg951insGlnGln
NM_006015.4:c.3998_4003dup , LRG_875t1:c.3998_4003dup NP_006006.3:p.Gln1334_Arg1335insGlnGln
NM_139135.2:c.3998_4003dup NP_624361.1:p.Gln1334_Arg1335insGlnGln
NM_006015.5:c.3998_4003dup NP_006006.3:p.Gln1334_Arg1335insGlnGln
NM_139135.3:c.3998_4003dup NP_624361.1:p.Gln1334_Arg1335insGlnGln
NM_006015.6:c.3998_4003dup MANE Select NP_006006.3:p.Gln1334_Arg1335insGlnGln
NM_139135.4:c.3998_4003dup NP_624361.1:p.Gln1334_Arg1335insGlnGln