Canonical Allele Identifier: CA645294042
Gene: ARID1B HGNC NCBI

Linked Data

ClinVar Variation Id: 426580
dbSNP Id: rs1085307695

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157133049_157133052del , CM000668.2:g.157133049_157133052del GRCh38
NC_000006.11:g.157454183_157454186del , CM000668.1:g.157454183_157454186del GRCh37
NC_000006.10:g.157495875_157495878del NCBI36
NG_032093.1:g.360120_360123del
NG_032093.2:g.360120_360123del
NG_066624.1:g.362024_362027del

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.2603_2606del ENSP00000055163.8:p.Arg868ThrfsTer?
ENST00000414678.8:c.2513_2516del ENSP00000412835.3:p.Arg838ThrfsTer?
ENST00000637015.2:c.2603_2606del ENSP00000489729.2:p.Arg868ThrfsTer?
ENST00000319584.11:c.617_620del ENSP00000313006.7:p.Arg206ThrfsTer?
ENST00000346085.10:c.2642_2645del ENSP00000344546.5:p.Arg881ThrfsTer?
ENST00000350026.10:c.2354_2357del ENSP00000055163.7:p.Arg785ThrfsTer?
ENST00000414678.7:c.761_764del ENSP00000412835.2:p.Arg254ThrfsTer?
ENST00000452544.2:n.504_507del
ENST00000635849.1:c.83-15575_83-15572del ENSP00000490948.1:n.83-15575_83-15572del
ENST00000636930.2:c.2603_2606del MANE Select ENSP00000490491.2:p.Arg868ThrfsTer?
ENST00000637003.1:c.104_107del ENSP00000489666.1:p.Arg35ThrfsTer?
ENST00000637810.1:c.104_107del ENSP00000489636.1:p.Arg35ThrfsTer?
ENST00000637904.1:c.104_107del ENSP00000490550.1:p.Arg35ThrfsTer?
ENST00000647938.1:c.2393_2396del ENSP00000498155.1:p.Arg798ThrfsTer?
ENST00000674190.1:n.1352_1355del
ENST00000319584.10:c.620_623del ENSP00000313006.6:p.Arg207ThrfsTer?
ENST00000346085.9:c.2393_2396del ENSP00000344546.4:p.Arg798ThrfsTer?
ENST00000350026.9:c.2354_2357del ENSP00000055163.7:p.Arg785ThrfsTer?
ENST00000414678.6:c.761_764del ENSP00000412835.2:p.Arg254ThrfsTer?
ENST00000452544.1:n.450_453del
NM_017519.2:c.2354_2357del NP_059989.2:p.Arg785ThrfsTer?
NM_020732.3:c.2393_2396del NP_065783.3:p.Arg798ThrfsTer?
XM_005267069.3:c.2354_2357del XP_005267126.2:p.Arg785ThrfsTer?
XM_011535984.1:c.1304_1307del XP_011534286.1:p.Arg435ThrfsTer?
XM_011535985.1:c.1283-15575_1283-15572del XP_011534287.1:n.1283-15575_1283-15572del...
XM_011535986.1:c.884_887del XP_011534288.1:p.Arg295ThrfsTer?
XM_011535987.1:c.503_506del XP_011534289.1:p.Arg168ThrfsTer?
NM_001346813.1:c.2354_2357del NP_001333742.1:p.Arg785ThrfsTer?
NM_001363725.1:c.104_107del NP_001350654.1:p.Arg35ThrfsTer?
XM_011535984.2:c.2435_2438del XP_011534286.2:p.Arg812ThrfsTer?
XM_017011103.2:c.2435_2438del XP_016866592.1:p.Arg812ThrfsTer?
XM_017011104.1:c.2435_2438del XP_016866593.1:p.Arg812ThrfsTer?
XM_017011105.2:c.2435_2438del XP_016866594.1:p.Arg812ThrfsTer?
XM_017011106.2:c.2435_2438del XP_016866595.1:p.Arg812ThrfsTer?
XM_017011107.2:c.2414-15575_2414-15572del XP_016866596.1:n.2414-15575_2414-15572del...
XR_002956289.1:n.2518_2521del
NM_001363725.2:c.104_107del NP_001350654.1:p.Arg35ThrfsTer?
NM_001371656.1:c.2642_2645del NP_001358585.1:p.Arg881ThrfsTer?
NM_001374820.1:c.2642_2645del NP_001361749.1:p.Arg881ThrfsTer?
NM_001374828.1:c.2603_2606del MANE Select NP_001361757.1:p.Arg868ThrfsTer?
NM_017519.3:c.2603_2606del NP_059989.3:p.Arg868ThrfsTer?