Canonical Allele Identifier: CA2695207268

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201016dup , CM000668.2:g.157201016dup	GRCh38
NC_000006.11:g.157522150dup , CM000668.1:g.157522150dup	GRCh37
NC_000006.10:g.157563842dup	NCBI36
NG_032093.1:g.428087dup
NG_032093.2:g.428087dup
NG_066624.1:g.429991dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4632dup	ENSP00000055163.8:p.Tyr1545LeufsTer?
ENST00000414678.8:c.4701dup	ENSP00000412835.3:p.Tyr1568LeufsTer?
ENST00000637015.2:c.4920dup	ENSP00000489729.2:p.Tyr1641LeufsTer?
ENST00000346085.10:c.4671dup	ENSP00000344546.5:p.Tyr1558LeufsTer?
ENST00000350026.10:c.4383dup	ENSP00000055163.7:p.Tyr1462LeufsTer?
ENST00000414678.7:c.2949dup	ENSP00000412835.2:p.Tyr984LeufsTer?
ENST00000635849.1:c.2112dup	ENSP00000490948.1:p.Tyr705LeufsTer?
ENST00000635957.1:c.1743dup	ENSP00000490385.1:p.Tyr582LeufsTer?
ENST00000636227.1:n.3254dup
ENST00000636254.1:n.711dup
ENST00000636930.2:c.4791dup MANE Select	ENSP00000490491.2:p.Tyr1598LeufsTer?
ENST00000636940.1:n.2788dup
ENST00000637015.1:c.2159dup
ENST00000637568.1:c.2073dup
ENST00000637741.1:n.1457dup
ENST00000637810.1:c.2133dup	ENSP00000489636.1:p.Tyr712LeufsTer?
ENST00000637904.1:c.2292dup	ENSP00000490550.1:p.Tyr765LeufsTer?
ENST00000647938.1:c.4422dup	ENSP00000498155.1:p.Tyr1475LeufsTer?
ENST00000346085.9:c.4422dup	ENSP00000344546.4:p.Tyr1475LeufsTer?
ENST00000350026.9:c.4383dup	ENSP00000055163.7:p.Tyr1462LeufsTer?
ENST00000414678.6:c.2949dup	ENSP00000412835.2:p.Tyr984LeufsTer?
NM_017519.2:c.4383dup	NP_059989.2:p.Tyr1462LeufsTer?
NM_020732.3:c.4422dup	NP_065783.3:p.Tyr1475LeufsTer?
XM_005267069.3:c.4542dup	XP_005267126.2:p.Tyr1515LeufsTer?
XM_011535984.1:c.3621dup	XP_011534286.1:p.Tyr1208LeufsTer?
XM_011535985.1:c.3441dup	XP_011534287.1:p.Tyr1148LeufsTer?
XM_011535986.1:c.3201dup	XP_011534288.1:p.Tyr1068LeufsTer?
XM_011535987.1:c.2820dup	XP_011534289.1:p.Tyr941LeufsTer?
XM_011535988.1:c.1683dup	XP_011534290.1:p.Tyr562LeufsTer?
NM_001346813.1:c.4542dup	NP_001333742.1:p.Tyr1515LeufsTer?
NM_001363725.1:c.2292dup	NP_001350654.1:p.Tyr765LeufsTer?
XM_011535984.2:c.4752dup	XP_011534286.2:p.Tyr1585LeufsTer?
XM_011535988.3:c.1683dup	XP_011534290.1:p.Tyr562LeufsTer?
XM_017011103.2:c.4653dup	XP_016866592.1:p.Tyr1552LeufsTer?
XM_017011104.1:c.4623dup	XP_016866593.1:p.Tyr1542LeufsTer?
XM_017011105.2:c.4593dup	XP_016866594.1:p.Tyr1532LeufsTer?
XM_017011106.2:c.4464dup	XP_016866595.1:p.Tyr1489LeufsTer?
XM_017011107.2:c.4443dup	XP_016866596.1:p.Tyr1482LeufsTer?
XR_002956289.1:n.4738dup
NM_001363725.2:c.2292dup	NP_001350654.1:p.Tyr765LeufsTer?
NM_001371656.1:c.4671dup	NP_001358585.1:p.Tyr1558LeufsTer?
NM_001374820.1:c.4671dup	NP_001361749.1:p.Tyr1558LeufsTer?
NM_001374828.1:c.4791dup MANE Select	NP_001361757.1:p.Tyr1598LeufsTer?
NM_017519.3:c.4632dup	NP_059989.3:p.Tyr1545LeufsTer?