Canonical Allele Identifier: CA2574277633
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696605_26696610del , CM000663.2:g.26696605_26696610del GRCh38
NC_000001.10:g.27023096_27023101del , CM000663.1:g.27023096_27023101del GRCh37
NC_000001.9:g.26895683_26895688del NCBI36
NG_029965.1:g.5575_5580del , LRG_875:g.5575_5580del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.202_207del MANE Select ENSP00000320485.7:p.Pro68_Leu69del
ENST00000430799.7:c.-13+2988_-13+2993del ENSP00000390317.3:n.-13+2988_-13+2993del
ENST00000637465.1:c.-13+505_-13+510del ENSP00000490650.1:n.-13+505_-13+510del
ENST00000324856.11:c.202_207del ENSP00000320485.7:p.Pro68_Leu69del
ENST00000457599.6:c.202_207del ENSP00000387636.2:p.Pro68_Leu69del
NM_006015.4:c.202_207del , LRG_875t1:c.202_207del NP_006006.3:p.Pro68_Leu69del
NM_139135.2:c.202_207del NP_624361.1:p.Pro68_Leu69del
NM_006015.5:c.202_207del NP_006006.3:p.Pro68_Leu69del
NM_139135.3:c.202_207del NP_624361.1:p.Pro68_Leu69del
NM_006015.6:c.202_207del MANE Select NP_006006.3:p.Pro68_Leu69del
NM_139135.4:c.202_207del NP_624361.1:p.Pro68_Leu69del