Canonical Allele Identifier: CA2742917363
Gene: ARID1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696666_26696679del , CM000663.2:g.26696666_26696679del GRCh38
NC_000001.10:g.27023157_27023170del , CM000663.1:g.27023157_27023170del GRCh37
NC_000001.9:g.26895744_26895757del NCBI36
NG_029965.1:g.5636_5649del , LRG_875:g.5636_5649del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.263_276del MANE Select ENSP00000320485.7:p.Ala88GlyfsTer18
ENST00000430799.7:c.-13+3049_-13+3062del ENSP00000390317.3:n.-13+3049_-13+3062del
ENST00000637465.1:c.-13+566_-13+579del ENSP00000490650.1:n.-13+566_-13+579del
ENST00000324856.11:c.263_276del ENSP00000320485.7:p.Ala88GlyfsTer18
ENST00000457599.6:c.263_276del ENSP00000387636.2:p.Ala88GlyfsTer18
NM_006015.4:c.263_276del , LRG_875t1:c.263_276del NP_006006.3:p.Ala88GlyfsTer18
NM_139135.2:c.263_276del NP_624361.1:p.Ala88GlyfsTer18
NM_006015.5:c.263_276del NP_006006.3:p.Ala88GlyfsTer18
NM_139135.3:c.263_276del NP_624361.1:p.Ala88GlyfsTer18
NM_006015.6:c.263_276del MANE Select NP_006006.3:p.Ala88GlyfsTer18
NM_139135.4:c.263_276del NP_624361.1:p.Ala88GlyfsTer18