Canonical Allele Identifier: CA2740090630
Gene: ARID1A HGNC NCBI

Linked Data

ClinVar Variation Id: 3010529
ClinVar RCV Id: RCV003862168
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696771_26696772delinsAG , CM000663.2:g.26696771_26696772delinsAG GRCh38
NC_000001.10:g.27023262_27023263delinsAG , CM000663.1:g.27023262_27023263delinsAG GRCh37
NC_000001.9:g.26895849_26895850delinsAG NCBI36
NG_029965.1:g.5741_5742delinsAG , LRG_875:g.5741_5742delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.368_369delinsAG MANE Select ENSP00000320485.7:p.Gly123Glu
ENST00000430799.7:c.-13+3154_-13+3155delinsAG ENSP00000390317.3:n.-13+3154_-13+3155delinsAG
ENST00000637465.1:c.-13+671_-13+672delinsAG ENSP00000490650.1:n.-13+671_-13+672delinsAG
ENST00000324856.11:c.368_369delinsAG ENSP00000320485.7:p.Gly123Glu
ENST00000457599.6:c.368_369delinsAG ENSP00000387636.2:p.Gly123Glu
NM_006015.4:c.368_369delinsAG , LRG_875t1:c.368_369delinsAG NP_006006.3:p.Gly123Glu
NM_139135.2:c.368_369delinsAG NP_624361.1:p.Gly123Glu
NM_006015.5:c.368_369delinsAG NP_006006.3:p.Gly123Glu
NM_139135.3:c.368_369delinsAG NP_624361.1:p.Gly123Glu
NM_006015.6:c.368_369delinsAG MANE Select NP_006006.3:p.Gly123Glu
NM_139135.4:c.368_369delinsAG NP_624361.1:p.Gly123Glu
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