Canonical Allele Identifier: CA2695687011
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs2124740877
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696638_26696639dup , CM000663.2:g.26696638_26696639dup GRCh38
NC_000001.10:g.27023129_27023130dup , CM000663.1:g.27023129_27023130dup GRCh37
NC_000001.9:g.26895716_26895717dup NCBI36
NG_029965.1:g.5608_5609dup , LRG_875:g.5608_5609dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.235_236dup MANE Select ENSP00000320485.7:p.Ser79ArgfsTer23
ENST00000430799.7:c.-13+3021_-13+3022dup ENSP00000390317.3:n.-13+3021_-13+3022dup
ENST00000637465.1:c.-13+538_-13+539dup ENSP00000490650.1:n.-13+538_-13+539dup
ENST00000324856.11:c.235_236dup ENSP00000320485.7:p.Ser79ArgfsTer23
ENST00000457599.6:c.235_236dup ENSP00000387636.2:p.Ser79ArgfsTer23
NM_006015.4:c.235_236dup , LRG_875t1:c.235_236dup NP_006006.3:p.Ser79ArgfsTer23
NM_139135.2:c.235_236dup NP_624361.1:p.Ser79ArgfsTer23
NM_006015.5:c.235_236dup NP_006006.3:p.Ser79ArgfsTer23
NM_139135.3:c.235_236dup NP_624361.1:p.Ser79ArgfsTer23
NM_006015.6:c.235_236dup MANE Select NP_006006.3:p.Ser79ArgfsTer23
NM_139135.4:c.235_236dup NP_624361.1:p.Ser79ArgfsTer23
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