Canonical Allele Identifier: CA2680892445

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190058-ACGACCCATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190060_157190068del , CM000668.2:g.157190060_157190068del	GRCh38
NC_000006.11:g.157511194_157511202del , CM000668.1:g.157511194_157511202del	GRCh37
NC_000006.10:g.157552886_157552894del	NCBI36
NG_032093.1:g.417131_417139del
NG_032093.2:g.417131_417139del
NG_066624.1:g.419035_419043del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3922_3930del	ENSP00000055163.8:p.Asp1308_Phe1310del
ENST00000414678.8:c.3991_3999del	ENSP00000412835.3:p.Asp1331_Phe1333del
ENST00000637015.2:c.4210_4218del	ENSP00000489729.2:p.Asp1404_Phe1406del
ENST00000346085.10:c.3961_3969del	ENSP00000344546.5:p.Asp1321_Phe1323del
ENST00000350026.10:c.3673_3681del	ENSP00000055163.7:p.Asp1225_Phe1227del
ENST00000414678.7:c.2239_2247del	ENSP00000412835.2:p.Asp747_Phe749del
ENST00000635849.1:c.1402_1410del	ENSP00000490948.1:p.Asp468_Phe470del
ENST00000635957.1:c.1033_1041del	ENSP00000490385.1:p.Asp345_Phe347del
ENST00000636930.2:c.4081_4089del MANE Select	ENSP00000490491.2:p.Asp1361_Phe1363del
ENST00000636940.1:n.2078_2086del
ENST00000637015.1:c.1449_1457del
ENST00000637568.1:c.1363_1371del
ENST00000637741.1:n.747_755del
ENST00000637810.1:c.1423_1431del	ENSP00000489636.1:p.Asp475_Phe477del
ENST00000637904.1:c.1582_1590del	ENSP00000490550.1:p.Asp528_Phe530del
ENST00000647938.1:c.3712_3720del	ENSP00000498155.1:p.Asp1238_Phe1240del
ENST00000346085.9:c.3712_3720del	ENSP00000344546.4:p.Asp1238_Phe1240del
ENST00000350026.9:c.3673_3681del	ENSP00000055163.7:p.Asp1225_Phe1227del
ENST00000414678.6:c.2239_2247del	ENSP00000412835.2:p.Asp747_Phe749del
NM_017519.2:c.3673_3681del	NP_059989.2:p.Asp1225_Phe1227del
NM_020732.3:c.3712_3720del	NP_065783.3:p.Asp1238_Phe1240del
XM_005267069.3:c.3832_3840del	XP_005267126.2:p.Asp1278_Phe1280del
XM_011535984.1:c.2911_2919del	XP_011534286.1:p.Asp971_Phe973del
XM_011535985.1:c.2731_2739del	XP_011534287.1:p.Asp911_Phe913del
XM_011535986.1:c.2491_2499del	XP_011534288.1:p.Asp831_Phe833del
XM_011535987.1:c.2110_2118del	XP_011534289.1:p.Asp704_Phe706del
XM_011535988.1:c.973_981del	XP_011534290.1:p.Asp325_Phe327del
NM_001346813.1:c.3832_3840del	NP_001333742.1:p.Asp1278_Phe1280del
NM_001363725.1:c.1582_1590del	NP_001350654.1:p.Asp528_Phe530del
XM_011535984.2:c.4042_4050del	XP_011534286.2:p.Asp1348_Phe1350del
XM_011535988.3:c.973_981del	XP_011534290.1:p.Asp325_Phe327del
XM_017011103.2:c.3943_3951del	XP_016866592.1:p.Asp1315_Phe1317del
XM_017011104.1:c.3913_3921del	XP_016866593.1:p.Asp1305_Phe1307del
XM_017011105.2:c.3883_3891del	XP_016866594.1:p.Asp1295_Phe1297del
XM_017011106.2:c.3754_3762del	XP_016866595.1:p.Asp1252_Phe1254del
XM_017011107.2:c.3733_3741del	XP_016866596.1:p.Asp1245_Phe1247del
XR_002956289.1:n.4125_4133del
NM_001363725.2:c.1582_1590del	NP_001350654.1:p.Asp528_Phe530del
NM_001371656.1:c.3961_3969del	NP_001358585.1:p.Asp1321_Phe1323del
NM_001374820.1:c.3961_3969del	NP_001361749.1:p.Asp1321_Phe1323del
NM_001374828.1:c.4081_4089del MANE Select	NP_001361757.1:p.Asp1361_Phe1363del
NM_017519.3:c.3922_3930del	NP_059989.3:p.Asp1308_Phe1310del