Canonical Allele Identifier: CA2739289478
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201323dup , CM000668.2:g.157201323dup GRCh38
NC_000006.11:g.157522457dup , CM000668.1:g.157522457dup GRCh37
NC_000006.10:g.157564149dup NCBI36
NG_032093.1:g.428394dup
NG_032093.2:g.428394dup
NG_066624.1:g.430298dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4939dup ENSP00000055163.8:p.Ser1647PhefsTer?
ENST00000414678.8:c.5008dup ENSP00000412835.3:p.Ser1670PhefsTer?
ENST00000637015.2:c.5227dup ENSP00000489729.2:p.Ser1743PhefsTer?
ENST00000346085.10:c.4978dup ENSP00000344546.5:p.Ser1660PhefsTer?
ENST00000350026.10:c.4690dup ENSP00000055163.7:p.Ser1564PhefsTer?
ENST00000414678.7:c.3256dup ENSP00000412835.2:p.Ser1086PhefsTer?
ENST00000635849.1:c.2419dup ENSP00000490948.1:p.Ser807PhefsTer?
ENST00000635957.1:c.2050dup ENSP00000490385.1:p.Ser684PhefsTer?
ENST00000636227.1:n.3561dup
ENST00000636254.1:n.1018dup
ENST00000636930.2:c.5098dup MANE Select ENSP00000490491.2:p.Ser1700PhefsTer?
ENST00000636940.1:n.3095dup
ENST00000637015.1:c.2466dup
ENST00000637568.1:c.2380dup
ENST00000637741.1:n.1764dup
ENST00000637810.1:c.2440dup ENSP00000489636.1:p.Ser814PhefsTer?
ENST00000637904.1:c.2599dup ENSP00000490550.1:p.Ser867PhefsTer?
ENST00000647938.1:c.4729dup ENSP00000498155.1:p.Ser1577PhefsTer?
ENST00000346085.9:c.4729dup ENSP00000344546.4:p.Ser1577PhefsTer?
ENST00000350026.9:c.4690dup ENSP00000055163.7:p.Ser1564PhefsTer?
ENST00000414678.6:c.3256dup ENSP00000412835.2:p.Ser1086PhefsTer?
NM_017519.2:c.4690dup NP_059989.2:p.Ser1564PhefsTer?
NM_020732.3:c.4729dup NP_065783.3:p.Ser1577PhefsTer?
XM_005267069.3:c.4849dup XP_005267126.2:p.Ser1617PhefsTer?
XM_011535984.1:c.3928dup XP_011534286.1:p.Ser1310PhefsTer?
XM_011535985.1:c.3748dup XP_011534287.1:p.Ser1250PhefsTer?
XM_011535986.1:c.3508dup XP_011534288.1:p.Ser1170PhefsTer?
XM_011535987.1:c.3127dup XP_011534289.1:p.Ser1043PhefsTer?
XM_011535988.1:c.1990dup XP_011534290.1:p.Ser664PhefsTer?
NM_001346813.1:c.4849dup NP_001333742.1:p.Ser1617PhefsTer?
NM_001363725.1:c.2599dup NP_001350654.1:p.Ser867PhefsTer?
XM_011535984.2:c.5059dup XP_011534286.2:p.Ser1687PhefsTer?
XM_011535988.3:c.1990dup XP_011534290.1:p.Ser664PhefsTer?
XM_017011103.2:c.4960dup XP_016866592.1:p.Ser1654PhefsTer?
XM_017011104.1:c.4930dup XP_016866593.1:p.Ser1644PhefsTer?
XM_017011105.2:c.4900dup XP_016866594.1:p.Ser1634PhefsTer?
XM_017011106.2:c.4771dup XP_016866595.1:p.Ser1591PhefsTer?
XM_017011107.2:c.4750dup XP_016866596.1:p.Ser1584PhefsTer?
XR_002956289.1:n.5045dup
NM_001363725.2:c.2599dup NP_001350654.1:p.Ser867PhefsTer?
NM_001371656.1:c.4978dup NP_001358585.1:p.Ser1660PhefsTer?
NM_001374820.1:c.4978dup NP_001361749.1:p.Ser1660PhefsTer?
NM_001374828.1:c.5098dup MANE Select NP_001361757.1:p.Ser1700PhefsTer?
NM_017519.3:c.4939dup NP_059989.3:p.Ser1647PhefsTer?