Canonical Allele Identifier: CA151061
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157200971del , CM000668.2:g.157200971del GRCh38
NC_000006.11:g.157522105del , CM000668.1:g.157522105del GRCh37
NC_000006.10:g.157563797del NCBI36
NG_032093.1:g.428042del
NG_032093.2:g.428042del
NG_066624.1:g.429946del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4587del ENSP00000055163.8:p.Pro1530LeufsTer?
ENST00000414678.8:c.4656del ENSP00000412835.3:p.Pro1553LeufsTer?
ENST00000637015.2:c.4875del ENSP00000489729.2:p.Pro1626LeufsTer?
ENST00000346085.10:c.4626del ENSP00000344546.5:p.Pro1543LeufsTer?
ENST00000350026.10:c.4338del ENSP00000055163.7:p.Pro1447LeufsTer?
ENST00000414678.7:c.2904del ENSP00000412835.2:p.Pro969LeufsTer?
ENST00000635849.1:c.2067del ENSP00000490948.1:p.Pro690LeufsTer?
ENST00000635957.1:c.1698del ENSP00000490385.1:p.Pro567LeufsTer?
ENST00000636227.1:n.3209del
ENST00000636254.1:n.666del
ENST00000636930.2:c.4746del MANE Select ENSP00000490491.2:p.Pro1583LeufsTer?
ENST00000636940.1:n.2743del
ENST00000637015.1:c.2114del
ENST00000637568.1:c.2028del
ENST00000637741.1:n.1412del
ENST00000637810.1:c.2088del ENSP00000489636.1:p.Pro697LeufsTer?
ENST00000637904.1:c.2247del ENSP00000490550.1:p.Pro750LeufsTer?
ENST00000647938.1:c.4377del ENSP00000498155.1:p.Pro1460LeufsTer?
ENST00000346085.9:c.4377del ENSP00000344546.4:p.Pro1460LeufsTer?
ENST00000350026.9:c.4338del ENSP00000055163.7:p.Pro1447LeufsTer?
ENST00000414678.6:c.2904del ENSP00000412835.2:p.Pro969LeufsTer?
NM_017519.2:c.4338del NP_059989.2:p.Pro1447LeufsTer?
NM_020732.3:c.4377del NP_065783.3:p.Pro1460LeufsTer?
XM_005267069.3:c.4497del XP_005267126.2:p.Pro1500LeufsTer?
XM_011535984.1:c.3576del XP_011534286.1:p.Pro1193LeufsTer?
XM_011535985.1:c.3396del XP_011534287.1:p.Pro1133LeufsTer?
XM_011535986.1:c.3156del XP_011534288.1:p.Pro1053LeufsTer?
XM_011535987.1:c.2775del XP_011534289.1:p.Pro926LeufsTer?
XM_011535988.1:c.1638del XP_011534290.1:p.Pro547LeufsTer?
NM_001346813.1:c.4497del NP_001333742.1:p.Pro1500LeufsTer?
NM_001363725.1:c.2247del NP_001350654.1:p.Pro750LeufsTer?
XM_011535984.2:c.4707del XP_011534286.2:p.Pro1570LeufsTer?
XM_011535988.3:c.1638del XP_011534290.1:p.Pro547LeufsTer?
XM_017011103.2:c.4608del XP_016866592.1:p.Pro1537LeufsTer?
XM_017011104.1:c.4578del XP_016866593.1:p.Pro1527LeufsTer?
XM_017011105.2:c.4548del XP_016866594.1:p.Pro1517LeufsTer?
XM_017011106.2:c.4419del XP_016866595.1:p.Pro1474LeufsTer?
XM_017011107.2:c.4398del XP_016866596.1:p.Pro1467LeufsTer?
XR_002956289.1:n.4693del
NM_001363725.2:c.2247del NP_001350654.1:p.Pro750LeufsTer?
NM_001371656.1:c.4626del NP_001358585.1:p.Pro1543LeufsTer?
NM_001374820.1:c.4626del NP_001361749.1:p.Pro1543LeufsTer?
NM_001374828.1:c.4746del MANE Select NP_001361757.1:p.Pro1583LeufsTer?
NM_017519.3:c.4587del NP_059989.3:p.Pro1530LeufsTer?