Canonical Allele Identifier: CA2837995139
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201195dup , CM000668.2:g.157201195dup GRCh38
NC_000006.11:g.157522329dup , CM000668.1:g.157522329dup GRCh37
NC_000006.10:g.157564021dup NCBI36
NG_032093.1:g.428266dup
NG_032093.2:g.428266dup
NG_066624.1:g.430170dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4811dup ENSP00000055163.8:p.Pro1606ThrfsTer?
ENST00000414678.8:c.4880dup ENSP00000412835.3:p.Pro1629ThrfsTer?
ENST00000637015.2:c.5099dup ENSP00000489729.2:p.Pro1702ThrfsTer?
ENST00000346085.10:c.4850dup ENSP00000344546.5:p.Pro1619ThrfsTer?
ENST00000350026.10:c.4562dup ENSP00000055163.7:p.Pro1523ThrfsTer?
ENST00000414678.7:c.3128dup ENSP00000412835.2:p.Pro1045ThrfsTer?
ENST00000635849.1:c.2291dup ENSP00000490948.1:p.Pro766ThrfsTer?
ENST00000635957.1:c.1922dup ENSP00000490385.1:p.Pro643ThrfsTer?
ENST00000636227.1:n.3433dup
ENST00000636254.1:n.890dup
ENST00000636930.2:c.4970dup MANE Select ENSP00000490491.2:p.Pro1659ThrfsTer?
ENST00000636940.1:n.2967dup
ENST00000637015.1:c.2338dup
ENST00000637568.1:c.2252dup
ENST00000637741.1:n.1636dup
ENST00000637810.1:c.2312dup ENSP00000489636.1:p.Pro773ThrfsTer?
ENST00000637904.1:c.2471dup ENSP00000490550.1:p.Pro826ThrfsTer?
ENST00000647938.1:c.4601dup ENSP00000498155.1:p.Pro1536ThrfsTer?
ENST00000346085.9:c.4601dup ENSP00000344546.4:p.Pro1536ThrfsTer?
ENST00000350026.9:c.4562dup ENSP00000055163.7:p.Pro1523ThrfsTer?
ENST00000414678.6:c.3128dup ENSP00000412835.2:p.Pro1045ThrfsTer?
NM_017519.2:c.4562dup NP_059989.2:p.Pro1523ThrfsTer?
NM_020732.3:c.4601dup NP_065783.3:p.Pro1536ThrfsTer?
XM_005267069.3:c.4721dup XP_005267126.2:p.Pro1576ThrfsTer?
XM_011535984.1:c.3800dup XP_011534286.1:p.Pro1269ThrfsTer?
XM_011535985.1:c.3620dup XP_011534287.1:p.Pro1209ThrfsTer?
XM_011535986.1:c.3380dup XP_011534288.1:p.Pro1129ThrfsTer?
XM_011535987.1:c.2999dup XP_011534289.1:p.Pro1002ThrfsTer?
XM_011535988.1:c.1862dup XP_011534290.1:p.Pro623ThrfsTer?
NM_001346813.1:c.4721dup NP_001333742.1:p.Pro1576ThrfsTer?
NM_001363725.1:c.2471dup NP_001350654.1:p.Pro826ThrfsTer?
XM_011535984.2:c.4931dup XP_011534286.2:p.Pro1646ThrfsTer?
XM_011535988.3:c.1862dup XP_011534290.1:p.Pro623ThrfsTer?
XM_017011103.2:c.4832dup XP_016866592.1:p.Pro1613ThrfsTer?
XM_017011104.1:c.4802dup XP_016866593.1:p.Pro1603ThrfsTer?
XM_017011105.2:c.4772dup XP_016866594.1:p.Pro1593ThrfsTer?
XM_017011106.2:c.4643dup XP_016866595.1:p.Pro1550ThrfsTer?
XM_017011107.2:c.4622dup XP_016866596.1:p.Pro1543ThrfsTer?
XR_002956289.1:n.4917dup
NM_001363725.2:c.2471dup NP_001350654.1:p.Pro826ThrfsTer?
NM_001371656.1:c.4850dup NP_001358585.1:p.Pro1619ThrfsTer?
NM_001374820.1:c.4850dup NP_001361749.1:p.Pro1619ThrfsTer?
NM_001374828.1:c.4970dup MANE Select NP_001361757.1:p.Pro1659ThrfsTer?
NM_017519.3:c.4811dup NP_059989.3:p.Pro1606ThrfsTer?