Canonical Allele Identifier: CA2695207256

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190066_157190067del , CM000668.2:g.157190066_157190067del	GRCh38
NC_000006.11:g.157511200_157511201del , CM000668.1:g.157511200_157511201del	GRCh37
NC_000006.10:g.157552892_157552893del	NCBI36
NG_032093.1:g.417137_417138del
NG_032093.2:g.417137_417138del
NG_066624.1:g.419041_419042del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3928_3929del	ENSP00000055163.8:p.Phe1310LeufsTer5
ENST00000414678.8:c.3997_3998del	ENSP00000412835.3:p.Phe1333LeufsTer5
ENST00000637015.2:c.4216_4217del	ENSP00000489729.2:p.Phe1406LeufsTer5
ENST00000346085.10:c.3967_3968del	ENSP00000344546.5:p.Phe1323LeufsTer5
ENST00000350026.10:c.3679_3680del	ENSP00000055163.7:p.Phe1227LeufsTer5
ENST00000414678.7:c.2245_2246del	ENSP00000412835.2:p.Phe749LeufsTer5
ENST00000635849.1:c.1408_1409del	ENSP00000490948.1:p.Phe470LeufsTer5
ENST00000635957.1:c.1039_1040del	ENSP00000490385.1:p.Phe347LeufsTer5
ENST00000636930.2:c.4087_4088del MANE Select	ENSP00000490491.2:p.Phe1363LeufsTer5
ENST00000636940.1:n.2084_2085del
ENST00000637015.1:c.1455_1456del
ENST00000637568.1:c.1369_1370del
ENST00000637741.1:n.753_754del
ENST00000637810.1:c.1429_1430del	ENSP00000489636.1:p.Phe477LeufsTer5
ENST00000637904.1:c.1588_1589del	ENSP00000490550.1:p.Phe530LeufsTer5
ENST00000647938.1:c.3718_3719del	ENSP00000498155.1:p.Phe1240LeufsTer5
ENST00000346085.9:c.3718_3719del	ENSP00000344546.4:p.Phe1240LeufsTer5
ENST00000350026.9:c.3679_3680del	ENSP00000055163.7:p.Phe1227LeufsTer5
ENST00000414678.6:c.2245_2246del	ENSP00000412835.2:p.Phe749LeufsTer5
NM_017519.2:c.3679_3680del	NP_059989.2:p.Phe1227LeufsTer5
NM_020732.3:c.3718_3719del	NP_065783.3:p.Phe1240LeufsTer5
XM_005267069.3:c.3838_3839del	XP_005267126.2:p.Phe1280LeufsTer5
XM_011535984.1:c.2917_2918del	XP_011534286.1:p.Phe973LeufsTer5
XM_011535985.1:c.2737_2738del	XP_011534287.1:p.Phe913LeufsTer5
XM_011535986.1:c.2497_2498del	XP_011534288.1:p.Phe833LeufsTer5
XM_011535987.1:c.2116_2117del	XP_011534289.1:p.Phe706LeufsTer5
XM_011535988.1:c.979_980del	XP_011534290.1:p.Phe327LeufsTer5
NM_001346813.1:c.3838_3839del	NP_001333742.1:p.Phe1280LeufsTer5
NM_001363725.1:c.1588_1589del	NP_001350654.1:p.Phe530LeufsTer5
XM_011535984.2:c.4048_4049del	XP_011534286.2:p.Phe1350LeufsTer5
XM_011535988.3:c.979_980del	XP_011534290.1:p.Phe327LeufsTer5
XM_017011103.2:c.3949_3950del	XP_016866592.1:p.Phe1317LeufsTer5
XM_017011104.1:c.3919_3920del	XP_016866593.1:p.Phe1307LeufsTer5
XM_017011105.2:c.3889_3890del	XP_016866594.1:p.Phe1297LeufsTer5
XM_017011106.2:c.3760_3761del	XP_016866595.1:p.Phe1254LeufsTer5
XM_017011107.2:c.3739_3740del	XP_016866596.1:p.Phe1247LeufsTer5
XR_002956289.1:n.4131_4132del
NM_001363725.2:c.1588_1589del	NP_001350654.1:p.Phe530LeufsTer5
NM_001371656.1:c.3967_3968del	NP_001358585.1:p.Phe1323LeufsTer5
NM_001374820.1:c.3967_3968del	NP_001361749.1:p.Phe1323LeufsTer5
NM_001374828.1:c.4087_4088del MANE Select	NP_001361757.1:p.Phe1363LeufsTer5
NM_017519.3:c.3928_3929del	NP_059989.3:p.Phe1310LeufsTer5