Canonical Allele Identifier: CA2773709214

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201403_157201404insCCCAACAC , CM000668.2:g.157201403_157201404insCCCAACAC	GRCh38
NC_000006.11:g.157522537_157522538insCCCAACAC , CM000668.1:g.157522537_157522538insCCCAACAC	GRCh37
NC_000006.10:g.157564229_157564230insCCCAACAC	NCBI36
NG_032093.1:g.428474_428475insCCCAACAC
NG_032093.2:g.428474_428475insCCCAACAC
NG_066624.1:g.430378_430379insCCCAACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5019_5020insCCCAACAC	ENSP00000055163.8:p.Arg1674ProfsTer13
ENST00000414678.8:c.5088_5089insCCCAACAC	ENSP00000412835.3:p.Arg1697ProfsTer13
ENST00000637015.2:c.5307_5308insCCCAACAC	ENSP00000489729.2:p.Arg1770ProfsTer13
ENST00000346085.10:c.5058_5059insCCCAACAC	ENSP00000344546.5:p.Arg1687ProfsTer13
ENST00000350026.10:c.4770_4771insCCCAACAC	ENSP00000055163.7:p.Arg1591ProfsTer13
ENST00000414678.7:c.3336_3337insCCCAACAC	ENSP00000412835.2:p.Arg1113ProfsTer13
ENST00000635849.1:c.2499_2500insCCCAACAC	ENSP00000490948.1:p.Arg834ProfsTer13
ENST00000635957.1:c.2130_2131insCCCAACAC	ENSP00000490385.1:p.Arg711ProfsTer13
ENST00000636227.1:n.3641_3642insCCCAACAC
ENST00000636254.1:n.1098_1099insCCCAACAC
ENST00000636930.2:c.5178_5179insCCCAACAC MANE Select	ENSP00000490491.2:p.Arg1727ProfsTer13
ENST00000636940.1:n.3175_3176insCCCAACAC
ENST00000637015.1:c.2546_2547insCCCAACAC
ENST00000637568.1:c.2460_2461insCCCAACAC
ENST00000637741.1:n.1844_1845insCCCAACAC
ENST00000637810.1:c.2520_2521insCCCAACAC	ENSP00000489636.1:p.Arg841ProfsTer13
ENST00000637904.1:c.2679_2680insCCCAACAC	ENSP00000490550.1:p.Arg894ProfsTer13
ENST00000647938.1:c.4809_4810insCCCAACAC	ENSP00000498155.1:p.Arg1604ProfsTer13
ENST00000346085.9:c.4809_4810insCCCAACAC	ENSP00000344546.4:p.Arg1604ProfsTer13
ENST00000350026.9:c.4770_4771insCCCAACAC	ENSP00000055163.7:p.Arg1591ProfsTer13
ENST00000414678.6:c.3336_3337insCCCAACAC	ENSP00000412835.2:p.Arg1113ProfsTer13
NM_017519.2:c.4770_4771insCCCAACAC	NP_059989.2:p.Arg1591ProfsTer13
NM_020732.3:c.4809_4810insCCCAACAC	NP_065783.3:p.Arg1604ProfsTer13
XM_005267069.3:c.4929_4930insCCCAACAC	XP_005267126.2:p.Arg1644ProfsTer13
XM_011535984.1:c.4008_4009insCCCAACAC	XP_011534286.1:p.Arg1337ProfsTer13
XM_011535985.1:c.3828_3829insCCCAACAC	XP_011534287.1:p.Arg1277ProfsTer13
XM_011535986.1:c.3588_3589insCCCAACAC	XP_011534288.1:p.Arg1197ProfsTer13
XM_011535987.1:c.3207_3208insCCCAACAC	XP_011534289.1:p.Arg1070ProfsTer13
XM_011535988.1:c.2070_2071insCCCAACAC	XP_011534290.1:p.Arg691ProfsTer13
NM_001346813.1:c.4929_4930insCCCAACAC	NP_001333742.1:p.Arg1644ProfsTer13
NM_001363725.1:c.2679_2680insCCCAACAC	NP_001350654.1:p.Arg894ProfsTer13
XM_011535984.2:c.5139_5140insCCCAACAC	XP_011534286.2:p.Arg1714ProfsTer13
XM_011535988.3:c.2070_2071insCCCAACAC	XP_011534290.1:p.Arg691ProfsTer13
XM_017011103.2:c.5040_5041insCCCAACAC	XP_016866592.1:p.Arg1681ProfsTer13
XM_017011104.1:c.5010_5011insCCCAACAC	XP_016866593.1:p.Arg1671ProfsTer13
XM_017011105.2:c.4980_4981insCCCAACAC	XP_016866594.1:p.Arg1661ProfsTer13
XM_017011106.2:c.4851_4852insCCCAACAC	XP_016866595.1:p.Arg1618ProfsTer13
XM_017011107.2:c.4830_4831insCCCAACAC	XP_016866596.1:p.Arg1611ProfsTer13
XR_002956289.1:n.5125_5126insCCCAACAC
NM_001363725.2:c.2679_2680insCCCAACAC	NP_001350654.1:p.Arg894ProfsTer13
NM_001371656.1:c.5058_5059insCCCAACAC	NP_001358585.1:p.Arg1687ProfsTer13
NM_001374820.1:c.5058_5059insCCCAACAC	NP_001361749.1:p.Arg1687ProfsTer13
NM_001374828.1:c.5178_5179insCCCAACAC MANE Select	NP_001361757.1:p.Arg1727ProfsTer13
NM_017519.3:c.5019_5020insCCCAACAC	NP_059989.3:p.Arg1674ProfsTer13