Canonical Allele Identifier: CA2574277637
Gene: ARID1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696670_26696671insGGT , CM000663.2:g.26696670_26696671insGGT GRCh38
NC_000001.10:g.27023161_27023162insGGT , CM000663.1:g.27023161_27023162insGGT GRCh37
NC_000001.9:g.26895748_26895749insGGT NCBI36
NG_029965.1:g.5640_5641insGGT , LRG_875:g.5640_5641insGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.267_268insGGT MANE Select ENSP00000320485.7:p.Gly89_Ser90insGly
ENST00000430799.7:c.-13+3053_-13+3054insGGT ENSP00000390317.3:n.-13+3053_-13+3054insGGT
ENST00000637465.1:c.-13+570_-13+571insGGT ENSP00000490650.1:n.-13+570_-13+571insGGT
ENST00000324856.11:c.267_268insGGT ENSP00000320485.7:p.Gly89_Ser90insGly
ENST00000457599.6:c.267_268insGGT ENSP00000387636.2:p.Gly89_Ser90insGly
NM_006015.4:c.267_268insGGT , LRG_875t1:c.267_268insGGT NP_006006.3:p.Gly89_Ser90insGly
NM_139135.2:c.267_268insGGT NP_624361.1:p.Gly89_Ser90insGly
NM_006015.5:c.267_268insGGT NP_006006.3:p.Gly89_Ser90insGly
NM_139135.3:c.267_268insGGT NP_624361.1:p.Gly89_Ser90insGly
NM_006015.6:c.267_268insGGT MANE Select NP_006006.3:p.Gly89_Ser90insGly
NM_139135.4:c.267_268insGGT NP_624361.1:p.Gly89_Ser90insGly
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