Canonical Allele Identifier: CA2644301426
Gene: ARID1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26779257_26779259del , CM000663.2:g.26779257_26779259del GRCh38
NC_000001.10:g.27105748_27105750del , CM000663.1:g.27105748_27105750del GRCh37
NC_000001.9:g.26978335_26978337del NCBI36
NG_029965.1:g.88227_88229del , LRG_875:g.88227_88229del

Transcript Alleles

HGVS Amino-acid change
ENST00000324856.13:c.5359_5361del MANE Select ENSP00000320485.7:p.Glu1787del
ENST00000374152.7:c.4210_4212del ENSP00000363267.2:p.Glu1404del
ENST00000430799.7:c.4207_4209del ENSP00000390317.3:p.Glu1403del
ENST00000466382.2:c.776_778del
ENST00000636219.1:c.4213_4215del ENSP00000489842.1:p.Glu1405del
ENST00000637788.1:n.1159_1161del
ENST00000324856.11:c.5359_5361del ENSP00000320485.7:p.Glu1787del
ENST00000374152.6:c.4210_4212del ENSP00000363267.2:p.Glu1404del
ENST00000430799.6:c.2048_2050del
ENST00000457599.6:c.4708_4710del ENSP00000387636.2:p.Glu1570del
ENST00000466382.1:c.776_778del
ENST00000532781.1:c.857_859del
NM_006015.4:c.5359_5361del , LRG_875t1:c.5359_5361del NP_006006.3:p.Glu1787del
NM_139135.2:c.4708_4710del NP_624361.1:p.Glu1570del
NM_006015.5:c.5359_5361del NP_006006.3:p.Glu1787del
NM_139135.3:c.4708_4710del NP_624361.1:p.Glu1570del
NM_006015.6:c.5359_5361del MANE Select NP_006006.3:p.Glu1787del
NM_139135.4:c.4708_4710del NP_624361.1:p.Glu1570del