Canonical Allele Identifier: CA913073608
Gene: ARID1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.27023142_27023143del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696652_26696653del , CM000663.2:g.26696652_26696653del GRCh38
NC_000001.10:g.27023143_27023144del , CM000663.1:g.27023143_27023144del GRCh37
NC_000001.9:g.26895730_26895731del NCBI36
NG_029965.1:g.5622_5623del , LRG_875:g.5622_5623del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.249_250del MANE Select ENSP00000320485.7:p.Gly84ArgfsTer26
ENST00000430799.7:c.-13+3035_-13+3036del ENSP00000390317.3:n.-13+3035_-13+3036del
ENST00000637465.1:c.-13+552_-13+553del ENSP00000490650.1:n.-13+552_-13+553del
ENST00000324856.11:c.249_250del ENSP00000320485.7:p.Gly84ArgfsTer26
ENST00000457599.6:c.249_250del ENSP00000387636.2:p.Gly84ArgfsTer26
NM_006015.4:c.249_250del , LRG_875t1:c.249_250del NP_006006.3:p.Gly84ArgfsTer26
NM_139135.2:c.249_250del NP_624361.1:p.Gly84ArgfsTer26
NM_006015.5:c.249_250del NP_006006.3:p.Gly84ArgfsTer26
NM_139135.3:c.249_250del NP_624361.1:p.Gly84ArgfsTer26
NM_006015.6:c.249_250del MANE Select NP_006006.3:p.Gly84ArgfsTer26
NM_139135.4:c.249_250del NP_624361.1:p.Gly84ArgfsTer26
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