Canonical Allele Identifier: CA2644294107
Gene: ARID1A HGNC NCBI

Linked Data

gnomAD v4: 1-26696680-G-GGT
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696681_26696682insTG , CM000663.2:g.26696681_26696682insTG GRCh38
NC_000001.10:g.27023172_27023173insTG , CM000663.1:g.27023172_27023173insTG GRCh37
NC_000001.9:g.26895759_26895760insTG NCBI36
NG_029965.1:g.5651_5652insTG , LRG_875:g.5651_5652insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.278_279insTG MANE Select ENSP00000320485.7:p.Pro94GlyfsTer8
ENST00000430799.7:c.-13+3064_-13+3065insTG ENSP00000390317.3:n.-13+3064_-13+3065insTG
ENST00000637465.1:c.-13+581_-13+582insTG ENSP00000490650.1:n.-13+581_-13+582insTG
ENST00000324856.11:c.278_279insTG ENSP00000320485.7:p.Pro94GlyfsTer8
ENST00000457599.6:c.278_279insTG ENSP00000387636.2:p.Pro94GlyfsTer8
NM_006015.4:c.278_279insTG , LRG_875t1:c.278_279insTG NP_006006.3:p.Pro94GlyfsTer8
NM_139135.2:c.278_279insTG NP_624361.1:p.Pro94GlyfsTer8
NM_006015.5:c.278_279insTG NP_006006.3:p.Pro94GlyfsTer8
NM_139135.3:c.278_279insTG NP_624361.1:p.Pro94GlyfsTer8
NM_006015.6:c.278_279insTG MANE Select NP_006006.3:p.Pro94GlyfsTer8
NM_139135.4:c.278_279insTG NP_624361.1:p.Pro94GlyfsTer8
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