Canonical Allele Identifier: CA208682
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157206294del , CM000668.2:g.157206294del GRCh38
NC_000006.11:g.157527428del , CM000668.1:g.157527428del GRCh37
NC_000006.10:g.157569120del NCBI36
NG_032093.1:g.433365del
NG_032093.2:g.433365del
NG_066624.1:g.435269del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.5363del ENSP00000055163.8:p.Lys1788ArgfsTer?
ENST00000414678.8:c.5432del ENSP00000412835.3:p.Lys1811ArgfsTer?
ENST00000637015.2:c.5651del ENSP00000489729.2:p.Lys1884ArgfsTer?
ENST00000346085.10:c.5402del ENSP00000344546.5:p.Lys1801ArgfsTer?
ENST00000350026.10:c.5114del ENSP00000055163.7:p.Lys1705ArgfsTer?
ENST00000414678.7:c.3680del ENSP00000412835.2:p.Lys1227ArgfsTer?
ENST00000635849.1:c.2843del ENSP00000490948.1:p.Lys948ArgfsTer?
ENST00000635957.1:c.2474del ENSP00000490385.1:p.Lys825ArgfsTer?
ENST00000636227.1:n.3985del
ENST00000636254.1:n.1442del
ENST00000636930.2:c.5522del MANE Select ENSP00000490491.2:p.Lys1841ArgfsTer?
ENST00000636940.1:n.3519del
ENST00000637015.1:c.2890del
ENST00000637568.1:c.2804del
ENST00000637741.1:n.2188del
ENST00000637810.1:c.2864del ENSP00000489636.1:p.Lys955ArgfsTer?
ENST00000637904.1:c.3023del ENSP00000490550.1:p.Lys1008ArgfsTer?
ENST00000637933.1:n.2637del
ENST00000647938.1:c.5153del ENSP00000498155.1:p.Lys1718ArgfsTer?
ENST00000346085.9:c.5153del ENSP00000344546.4:p.Lys1718ArgfsTer?
ENST00000350026.9:c.5114del ENSP00000055163.7:p.Lys1705ArgfsTer?
ENST00000414678.6:c.3680del ENSP00000412835.2:p.Lys1227ArgfsTer?
NM_017519.2:c.5114del NP_059989.2:p.Lys1705ArgfsTer?
NM_020732.3:c.5153del NP_065783.3:p.Lys1718ArgfsTer?
XM_005267069.3:c.5273del XP_005267126.2:p.Lys1758ArgfsTer?
XM_011535984.1:c.4352del XP_011534286.1:p.Lys1451ArgfsTer?
XM_011535985.1:c.4172del XP_011534287.1:p.Lys1391ArgfsTer?
XM_011535986.1:c.3932del XP_011534288.1:p.Lys1311ArgfsTer?
XM_011535987.1:c.3551del XP_011534289.1:p.Lys1184ArgfsTer?
XM_011535988.1:c.2414del XP_011534290.1:p.Lys805ArgfsTer?
NM_001346813.1:c.5273del NP_001333742.1:p.Lys1758ArgfsTer?
NM_001363725.1:c.3023del NP_001350654.1:p.Lys1008ArgfsTer?
XM_011535984.2:c.5483del XP_011534286.2:p.Lys1828ArgfsTer?
XM_011535988.3:c.2414del XP_011534290.1:p.Lys805ArgfsTer?
XM_017011103.2:c.5384del XP_016866592.1:p.Lys1795ArgfsTer?
XM_017011104.1:c.5354del XP_016866593.1:p.Lys1785ArgfsTer?
XM_017011105.2:c.5324del XP_016866594.1:p.Lys1775ArgfsTer?
XM_017011106.2:c.5195del XP_016866595.1:p.Lys1732ArgfsTer?
XM_017011107.2:c.5174del XP_016866596.1:p.Lys1725ArgfsTer?
XR_002956289.1:n.5469del
NM_001363725.2:c.3023del NP_001350654.1:p.Lys1008ArgfsTer?
NM_001371656.1:c.5402del NP_001358585.1:p.Lys1801ArgfsTer?
NM_001374820.1:c.5402del NP_001361749.1:p.Lys1801ArgfsTer?
NM_001374828.1:c.5522del MANE Select NP_001361757.1:p.Lys1841ArgfsTer?
NM_017519.3:c.5363del NP_059989.3:p.Lys1788ArgfsTer?