Canonical Allele Identifier: CA10584014
Gene: ARID1B HGNC NCBI

Linked Data

ClinVar Variation Id: 242866
dbSNP Id: rs879253746

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157200867dup , CM000668.2:g.157200867dup GRCh38
NC_000006.11:g.157522001dup , CM000668.1:g.157522001dup GRCh37
NC_000006.10:g.157563693dup NCBI36
NG_032093.1:g.427938dup
NG_032093.2:g.427938dup
NG_066624.1:g.429842dup

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.4483dup ENSP00000055163.8:p.Tyr1495LeufsTer?
ENST00000414678.8:c.4552dup ENSP00000412835.3:p.Tyr1518LeufsTer?
ENST00000637015.2:c.4771dup ENSP00000489729.2:p.Tyr1591LeufsTer?
ENST00000346085.10:c.4522dup ENSP00000344546.5:p.Tyr1508LeufsTer?
ENST00000350026.10:c.4234dup ENSP00000055163.7:p.Tyr1412LeufsTer?
ENST00000414678.7:c.2800dup ENSP00000412835.2:p.Tyr934LeufsTer?
ENST00000635849.1:c.1963dup ENSP00000490948.1:p.Tyr655LeufsTer?
ENST00000635957.1:c.1594dup ENSP00000490385.1:p.Tyr532LeufsTer?
ENST00000636227.1:n.3105dup
ENST00000636254.1:n.562dup
ENST00000636930.2:c.4642dup MANE Select ENSP00000490491.2:p.Tyr1548LeufsTer?
ENST00000636940.1:n.2639dup
ENST00000637015.1:c.2010dup
ENST00000637568.1:c.1924dup
ENST00000637741.1:n.1308dup
ENST00000637810.1:c.1984dup ENSP00000489636.1:p.Tyr662LeufsTer?
ENST00000637904.1:c.2143dup ENSP00000490550.1:p.Tyr715LeufsTer?
ENST00000647938.1:c.4273dup ENSP00000498155.1:p.Tyr1425LeufsTer?
ENST00000346085.9:c.4273dup ENSP00000344546.4:p.Tyr1425LeufsTer?
ENST00000350026.9:c.4234dup ENSP00000055163.7:p.Tyr1412LeufsTer?
ENST00000414678.6:c.2800dup ENSP00000412835.2:p.Tyr934LeufsTer?
NM_017519.2:c.4234dup NP_059989.2:p.Tyr1412LeufsTer?
NM_020732.3:c.4273dup NP_065783.3:p.Tyr1425LeufsTer?
XM_005267069.3:c.4393dup XP_005267126.2:p.Tyr1465LeufsTer?
XM_011535984.1:c.3472dup XP_011534286.1:p.Tyr1158LeufsTer?
XM_011535985.1:c.3292dup XP_011534287.1:p.Tyr1098LeufsTer?
XM_011535986.1:c.3052dup XP_011534288.1:p.Tyr1018LeufsTer?
XM_011535987.1:c.2671dup XP_011534289.1:p.Tyr891LeufsTer?
XM_011535988.1:c.1534dup XP_011534290.1:p.Tyr512LeufsTer?
NM_001346813.1:c.4393dup NP_001333742.1:p.Tyr1465LeufsTer?
NM_001363725.1:c.2143dup NP_001350654.1:p.Tyr715LeufsTer?
XM_011535984.2:c.4603dup XP_011534286.2:p.Tyr1535LeufsTer?
XM_011535988.3:c.1534dup XP_011534290.1:p.Tyr512LeufsTer?
XM_017011103.2:c.4504dup XP_016866592.1:p.Tyr1502LeufsTer?
XM_017011104.1:c.4474dup XP_016866593.1:p.Tyr1492LeufsTer?
XM_017011105.2:c.4444dup XP_016866594.1:p.Tyr1482LeufsTer?
XM_017011106.2:c.4315dup XP_016866595.1:p.Tyr1439LeufsTer?
XM_017011107.2:c.4294dup XP_016866596.1:p.Tyr1432LeufsTer?
XR_002956289.1:n.4589dup
NM_001363725.2:c.2143dup NP_001350654.1:p.Tyr715LeufsTer?
NM_001371656.1:c.4522dup NP_001358585.1:p.Tyr1508LeufsTer?
NM_001374820.1:c.4522dup NP_001361749.1:p.Tyr1508LeufsTer?
NM_001374828.1:c.4642dup MANE Select NP_001361757.1:p.Tyr1548LeufsTer?
NM_017519.3:c.4483dup NP_059989.3:p.Tyr1495LeufsTer?