Canonical Allele Identifier: CA2573140706
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157184343del , CM000668.2:g.157184343del GRCh38
NC_000006.11:g.157505477del , CM000668.1:g.157505477del GRCh37
NC_000006.10:g.157547169del NCBI36
NG_032093.1:g.411414del
NG_032093.2:g.411414del
NG_066624.1:g.413318del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3668del ENSP00000055163.8:p.Glu1223GlyfsTer?
ENST00000414678.8:c.3737del ENSP00000412835.3:p.Glu1246GlyfsTer?
ENST00000637015.2:c.3956del ENSP00000489729.2:p.Glu1319GlyfsTer?
ENST00000319584.11:c.1841del ENSP00000313006.7:p.Glu614GlyfsTer?
ENST00000346085.10:c.3707del ENSP00000344546.5:p.Glu1236GlyfsTer?
ENST00000350026.10:c.3419del ENSP00000055163.7:p.Glu1140GlyfsTer?
ENST00000414678.7:c.1985del ENSP00000412835.2:p.Glu662GlyfsTer?
ENST00000635849.1:c.1148del ENSP00000490948.1:p.Glu383GlyfsTer?
ENST00000635957.1:c.782del ENSP00000490385.1:p.Glu261GlyfsTer?
ENST00000636930.2:c.3827del MANE Select ENSP00000490491.2:p.Glu1276GlyfsTer?
ENST00000636940.1:n.1824del
ENST00000637015.1:c.1195del
ENST00000637568.1:c.1109del
ENST00000637741.1:n.493del
ENST00000637810.1:c.1169del ENSP00000489636.1:p.Glu390GlyfsTer?
ENST00000637904.1:c.1328del ENSP00000490550.1:p.Glu443GlyfsTer?
ENST00000647938.1:c.3458del ENSP00000498155.1:p.Glu1153GlyfsTer?
ENST00000319584.10:c.1844del ENSP00000313006.6:p.Glu615GlyfsTer?
ENST00000346085.9:c.3458del ENSP00000344546.4:p.Glu1153GlyfsTer?
ENST00000350026.9:c.3419del ENSP00000055163.7:p.Glu1140GlyfsTer?
ENST00000400790.3:c.620del ENSP00000383596.3:p.Glu207GlyfsTer?
ENST00000414678.6:c.1985del ENSP00000412835.2:p.Glu662GlyfsTer?
NM_017519.2:c.3419del NP_059989.2:p.Glu1140GlyfsTer?
NM_020732.3:c.3458del NP_065783.3:p.Glu1153GlyfsTer?
XM_005267069.3:c.3578del XP_005267126.2:p.Glu1193GlyfsTer?
XM_011535984.1:c.2657del XP_011534286.1:p.Glu886GlyfsTer?
XM_011535985.1:c.2477del XP_011534287.1:p.Glu826GlyfsTer?
XM_011535986.1:c.2237del XP_011534288.1:p.Glu746GlyfsTer?
XM_011535987.1:c.1856del XP_011534289.1:p.Glu619GlyfsTer?
XM_011535988.1:c.719del XP_011534290.1:p.Glu240GlyfsTer?
NM_001346813.1:c.3578del NP_001333742.1:p.Glu1193GlyfsTer?
NM_001363725.1:c.1328del NP_001350654.1:p.Glu443GlyfsTer?
XM_011535984.2:c.3788del XP_011534286.2:p.Glu1263GlyfsTer?
XM_011535988.3:c.719del XP_011534290.1:p.Glu240GlyfsTer?
XM_017011103.2:c.3689del XP_016866592.1:p.Glu1230GlyfsTer?
XM_017011104.1:c.3659del XP_016866593.1:p.Glu1220GlyfsTer?
XM_017011105.2:c.3629del XP_016866594.1:p.Glu1210GlyfsTer?
XM_017011106.2:c.3500del XP_016866595.1:p.Glu1167GlyfsTer?
XM_017011107.2:c.3479del XP_016866596.1:p.Glu1160GlyfsTer?
XR_002956289.1:n.3871del
NM_001363725.2:c.1328del NP_001350654.1:p.Glu443GlyfsTer?
NM_001371656.1:c.3707del NP_001358585.1:p.Glu1236GlyfsTer?
NM_001374820.1:c.3707del NP_001361749.1:p.Glu1236GlyfsTer?
NM_001374828.1:c.3827del MANE Select NP_001361757.1:p.Glu1276GlyfsTer?
NM_017519.3:c.3668del NP_059989.3:p.Glu1223GlyfsTer?