Canonical Allele Identifier: CA2680892114
Gene: ARID1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189797_157189798insA , CM000668.2:g.157189797_157189798insA GRCh38
NC_000006.11:g.157510931_157510932insA , CM000668.1:g.157510931_157510932insA GRCh37
NC_000006.10:g.157552623_157552624insA NCBI36
NG_032093.1:g.416868_416869insA
NG_032093.2:g.416868_416869insA
NG_066624.1:g.418772_418773insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3899+17_3899+18insA ENSP00000055163.8:n.3899+17_3899+18insA
ENST00000414678.8:c.3968+17_3968+18insA ENSP00000412835.3:n.3968+17_3968+18insA
ENST00000637015.2:c.4187+17_4187+18insA ENSP00000489729.2:n.4187+17_4187+18insA
ENST00000346085.10:c.3938+17_3938+18insA ENSP00000344546.5:n.3938+17_3938+18insA
ENST00000350026.10:c.3650+17_3650+18insA ENSP00000055163.7:n.3650+17_3650+18insA
ENST00000414678.7:c.2216+17_2216+18insA ENSP00000412835.2:n.2216+17_2216+18insA
ENST00000635849.1:c.1379+17_1379+18insA ENSP00000490948.1:n.1379+17_1379+18insA
ENST00000635957.1:c.1013+17_1013+18insA ENSP00000490385.1:n.1013+17_1013+18insA
ENST00000636930.2:c.4058+17_4058+18insA MANE Select ENSP00000490491.2:n.4058+17_4058+18insA
ENST00000636940.1:n.2055+17_2055+18insA
ENST00000637015.1:c.1426+17_1426+18insA
ENST00000637568.1:c.1340+17_1340+18insA
ENST00000637741.1:n.724+17_724+18insA
ENST00000637810.1:c.1400+17_1400+18insA ENSP00000489636.1:n.1400+17_1400+18insA
ENST00000637904.1:c.1559+17_1559+18insA ENSP00000490550.1:n.1559+17_1559+18insA
ENST00000647938.1:c.3689+17_3689+18insA ENSP00000498155.1:n.3689+17_3689+18insA
ENST00000346085.9:c.3689+17_3689+18insA ENSP00000344546.4:n.3689+17_3689+18insA
ENST00000350026.9:c.3650+17_3650+18insA ENSP00000055163.7:n.3650+17_3650+18insA
ENST00000414678.6:c.2216+17_2216+18insA ENSP00000412835.2:n.2216+17_2216+18insA
NM_017519.2:c.3650+17_3650+18insA NP_059989.2:n.3650+17_3650+18insA
NM_020732.3:c.3689+17_3689+18insA NP_065783.3:n.3689+17_3689+18insA
XM_005267069.3:c.3809+17_3809+18insA XP_005267126.2:n.3809+17_3809+18insA
XM_011535984.1:c.2888+17_2888+18insA XP_011534286.1:n.2888+17_2888+18insA
XM_011535985.1:c.2708+17_2708+18insA XP_011534287.1:n.2708+17_2708+18insA
XM_011535986.1:c.2468+17_2468+18insA XP_011534288.1:n.2468+17_2468+18insA
XM_011535987.1:c.2087+17_2087+18insA XP_011534289.1:n.2087+17_2087+18insA
XM_011535988.1:c.950+17_950+18insA XP_011534290.1:n.950+17_950+18insA
NM_001346813.1:c.3809+17_3809+18insA NP_001333742.1:n.3809+17_3809+18insA
NM_001363725.1:c.1559+17_1559+18insA NP_001350654.1:n.1559+17_1559+18insA
XM_011535984.2:c.4019+17_4019+18insA XP_011534286.2:n.4019+17_4019+18insA
XM_011535988.3:c.950+17_950+18insA XP_011534290.1:n.950+17_950+18insA
XM_017011103.2:c.3920+17_3920+18insA XP_016866592.1:n.3920+17_3920+18insA
XM_017011104.1:c.3890+17_3890+18insA XP_016866593.1:n.3890+17_3890+18insA
XM_017011105.2:c.3860+17_3860+18insA XP_016866594.1:n.3860+17_3860+18insA
XM_017011106.2:c.3731+17_3731+18insA XP_016866595.1:n.3731+17_3731+18insA
XM_017011107.2:c.3710+17_3710+18insA XP_016866596.1:n.3710+17_3710+18insA
XR_002956289.1:n.4102+17_4102+18insA
NM_001363725.2:c.1559+17_1559+18insA NP_001350654.1:n.1559+17_1559+18insA
NM_001371656.1:c.3938+17_3938+18insA NP_001358585.1:n.3938+17_3938+18insA
NM_001374820.1:c.3938+17_3938+18insA NP_001361749.1:n.3938+17_3938+18insA
NM_001374828.1:c.4058+17_4058+18insA MANE Select NP_001361757.1:n.4058+17_4058+18insA
NM_017519.3:c.3899+17_3899+18insA NP_059989.3:n.3899+17_3899+18insA