Canonical Allele Identifier: CA1675538381

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190045_157190049delinsACAAT , CM000668.2:g.157190045_157190049delinsACAAT	GRCh38
NC_000006.11:g.157511179_157511183delinsACAAT , CM000668.1:g.157511179_157511183delinsACAAT	GRCh37
NC_000006.10:g.157552871_157552875delinsACAAT	NCBI36
NG_032093.1:g.417116_417120delinsACAAT
NG_032093.2:g.417116_417120delinsACAAT
NG_066624.1:g.419020_419024delinsACAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3907_3911delinsACAAT	ENSP00000055163.8:p.Thr1303=
ENST00000414678.8:c.3976_3980delinsACAAT	ENSP00000412835.3:p.Thr1326=
ENST00000637015.2:c.4195_4199delinsACAAT	ENSP00000489729.2:p.Thr1399=
ENST00000346085.10:c.3946_3950delinsACAAT	ENSP00000344546.5:p.Thr1316=
ENST00000350026.10:c.3658_3662delinsACAAT	ENSP00000055163.7:p.Thr1220=
ENST00000414678.7:c.2224_2228delinsACAAT	ENSP00000412835.2:p.Thr742=
ENST00000635849.1:c.1387_1391delinsACAAT	ENSP00000490948.1:p.Thr463=
ENST00000635957.1:c.1018_1022delinsACAAT	ENSP00000490385.1:p.Thr340=
ENST00000636930.2:c.4066_4070delinsACAAT MANE Select	ENSP00000490491.2:p.Thr1356=
ENST00000636940.1:n.2063_2067delinsACAAT
ENST00000637015.1:c.1434_1438delinsACAAT
ENST00000637568.1:c.1348_1352delinsACAAT
ENST00000637741.1:n.732_736delinsACAAT
ENST00000637810.1:c.1408_1412delinsACAAT	ENSP00000489636.1:p.Thr470=
ENST00000637904.1:c.1567_1571delinsACAAT	ENSP00000490550.1:p.Thr523=
ENST00000647938.1:c.3697_3701delinsACAAT	ENSP00000498155.1:p.Thr1233=
ENST00000346085.9:c.3697_3701delinsACAAT	ENSP00000344546.4:p.Thr1233=
ENST00000350026.9:c.3658_3662delinsACAAT	ENSP00000055163.7:p.Thr1220=
ENST00000414678.6:c.2224_2228delinsACAAT	ENSP00000412835.2:p.Thr742=
NM_017519.2:c.3658_3662delinsACAAT	NP_059989.2:p.Thr1220=
NM_020732.3:c.3697_3701delinsACAAT	NP_065783.3:p.Thr1233=
XM_005267069.3:c.3817_3821delinsACAAT	XP_005267126.2:p.Thr1273=
XM_011535984.1:c.2896_2900delinsACAAT	XP_011534286.1:p.Thr966=
XM_011535985.1:c.2716_2720delinsACAAT	XP_011534287.1:p.Thr906=
XM_011535986.1:c.2476_2480delinsACAAT	XP_011534288.1:p.Thr826=
XM_011535987.1:c.2095_2099delinsACAAT	XP_011534289.1:p.Thr699=
XM_011535988.1:c.958_962delinsACAAT	XP_011534290.1:p.Thr320=
NM_001346813.1:c.3817_3821delinsACAAT	NP_001333742.1:p.Thr1273=
NM_001363725.1:c.1567_1571delinsACAAT	NP_001350654.1:p.Thr523=
XM_011535984.2:c.4027_4031delinsACAAT	XP_011534286.2:p.Thr1343=
XM_011535988.3:c.958_962delinsACAAT	XP_011534290.1:p.Thr320=
XM_017011103.2:c.3928_3932delinsACAAT	XP_016866592.1:p.Thr1310=
XM_017011104.1:c.3898_3902delinsACAAT	XP_016866593.1:p.Thr1300=
XM_017011105.2:c.3868_3872delinsACAAT	XP_016866594.1:p.Thr1290=
XM_017011106.2:c.3739_3743delinsACAAT	XP_016866595.1:p.Thr1247=
XM_017011107.2:c.3718_3722delinsACAAT	XP_016866596.1:p.Thr1240=
XR_002956289.1:n.4110_4114delinsACAAT
NM_001363725.2:c.1567_1571delinsACAAT	NP_001350654.1:p.Thr523=
NM_001371656.1:c.3946_3950delinsACAAT	NP_001358585.1:p.Thr1316=
NM_001374820.1:c.3946_3950delinsACAAT	NP_001361749.1:p.Thr1316=
NM_001374828.1:c.4066_4070delinsACAAT MANE Select	NP_001361757.1:p.Thr1356=
NM_017519.3:c.3907_3911delinsACAAT	NP_059989.3:p.Thr1303=