Canonical Allele Identifier: CA10575557
Gene: ARID1B HGNC NCBI

Linked Data

ClinVar Variation Id: 31211
dbSNP Id: rs876657380

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157181156_157181157del , CM000668.2:g.157181156_157181157del GRCh38
NC_000006.11:g.157502290_157502291del , CM000668.1:g.157502290_157502291del GRCh37
NC_000006.10:g.157543982_157543983del NCBI36
NG_032093.1:g.408227_408228del
NG_032093.2:g.408227_408228del
NG_066624.1:g.410131_410132del

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.3533_3534del ENSP00000055163.8:p.Lys1178ArgfsTer9
ENST00000414678.8:c.3602_3603del ENSP00000412835.3:p.Lys1201ArgfsTer9
ENST00000637015.2:c.3821_3822del ENSP00000489729.2:p.Lys1274ArgfsTer9
ENST00000319584.11:c.1706_1707del ENSP00000313006.7:p.Lys569ArgfsTer9
ENST00000346085.10:c.3572_3573del ENSP00000344546.5:p.Lys1191ArgfsTer9
ENST00000350026.10:c.3284_3285del ENSP00000055163.7:p.Lys1095ArgfsTer9
ENST00000414678.7:c.1850_1851del ENSP00000412835.2:p.Lys617ArgfsTer9
ENST00000635849.1:c.1013_1014del ENSP00000490948.1:p.Lys338ArgfsTer9
ENST00000635957.1:c.647_648del ENSP00000490385.1:p.Lys216ArgfsTer9
ENST00000636930.2:c.3692_3693del MANE Select ENSP00000490491.2:p.Lys1231ArgfsTer9
ENST00000636940.1:n.1689_1690del
ENST00000637015.1:c.1060_1061del
ENST00000637568.1:c.974_975del
ENST00000637741.1:n.358_359del
ENST00000637810.1:c.1034_1035del ENSP00000489636.1:p.Lys345ArgfsTer9
ENST00000637904.1:c.1193_1194del ENSP00000490550.1:p.Lys398ArgfsTer9
ENST00000647938.1:c.3323_3324del ENSP00000498155.1:p.Lys1108ArgfsTer9
ENST00000319584.10:c.1709_1710del ENSP00000313006.6:p.Lys570ArgfsTer9
ENST00000346085.9:c.3323_3324del ENSP00000344546.4:p.Lys1108ArgfsTer9
ENST00000350026.9:c.3284_3285del ENSP00000055163.7:p.Lys1095ArgfsTer9
ENST00000400790.3:c.485_486del ENSP00000383596.3:p.Lys162ArgfsTer9
ENST00000414678.6:c.1850_1851del ENSP00000412835.2:p.Lys617ArgfsTer9
ENST00000478761.3:c.894_895del
NM_017519.2:c.3284_3285del NP_059989.2:p.Lys1095ArgfsTer9
NM_020732.3:c.3323_3324del NP_065783.3:p.Lys1108ArgfsTer9
XM_005267069.3:c.3443_3444del XP_005267126.2:p.Lys1148ArgfsTer9
XM_011535984.1:c.2522_2523del XP_011534286.1:p.Lys841ArgfsTer9
XM_011535985.1:c.2342_2343del XP_011534287.1:p.Lys781ArgfsTer9
XM_011535986.1:c.2102_2103del XP_011534288.1:p.Lys701ArgfsTer9
XM_011535987.1:c.1721_1722del XP_011534289.1:p.Lys574ArgfsTer9
XM_011535988.1:c.584_585del XP_011534290.1:p.Lys195ArgfsTer9
NM_001346813.1:c.3443_3444del NP_001333742.1:p.Lys1148ArgfsTer9
NM_001363725.1:c.1193_1194del NP_001350654.1:p.Lys398ArgfsTer9
XM_011535984.2:c.3653_3654del XP_011534286.2:p.Lys1218ArgfsTer9
XM_011535988.3:c.584_585del XP_011534290.1:p.Lys195ArgfsTer9
XM_017011103.2:c.3554_3555del XP_016866592.1:p.Lys1185ArgfsTer9
XM_017011104.1:c.3524_3525del XP_016866593.1:p.Lys1175ArgfsTer9
XM_017011105.2:c.3494_3495del XP_016866594.1:p.Lys1165ArgfsTer9
XM_017011106.2:c.3365_3366del XP_016866595.1:p.Lys1122ArgfsTer9
XM_017011107.2:c.3344_3345del XP_016866596.1:p.Lys1115ArgfsTer9
XR_002956289.1:n.3736_3737del
NM_001363725.2:c.1193_1194del NP_001350654.1:p.Lys398ArgfsTer9
NM_001371656.1:c.3572_3573del NP_001358585.1:p.Lys1191ArgfsTer9
NM_001374820.1:c.3572_3573del NP_001361749.1:p.Lys1191ArgfsTer9
NM_001374828.1:c.3692_3693del MANE Select NP_001361757.1:p.Lys1231ArgfsTer9
NM_017519.3:c.3533_3534del NP_059989.3:p.Lys1178ArgfsTer9