Canonical Allele Identifier: CA2773709209

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201395_157201396insAAACACACCCAACA , CM000668.2:g.157201395_157201396insAAACACACCCAACA	GRCh38
NC_000006.11:g.157522529_157522530insAAACACACCCAACA , CM000668.1:g.157522529_157522530insAAACACACCCAACA	GRCh37
NC_000006.10:g.157564221_157564222insAAACACACCCAACA	NCBI36
NG_032093.1:g.428466_428467insAAACACACCCAACA
NG_032093.2:g.428466_428467insAAACACACCCAACA
NG_066624.1:g.430370_430371insAAACACACCCAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5011_5012insAAACACACCCAACA	ENSP00000055163.8:p.Pro1671GlnfsTer18
ENST00000414678.8:c.5080_5081insAAACACACCCAACA	ENSP00000412835.3:p.Pro1694GlnfsTer18
ENST00000637015.2:c.5299_5300insAAACACACCCAACA	ENSP00000489729.2:p.Pro1767GlnfsTer18
ENST00000346085.10:c.5050_5051insAAACACACCCAACA	ENSP00000344546.5:p.Pro1684GlnfsTer18
ENST00000350026.10:c.4762_4763insAAACACACCCAACA	ENSP00000055163.7:p.Pro1588GlnfsTer18
ENST00000414678.7:c.3328_3329insAAACACACCCAACA	ENSP00000412835.2:p.Pro1110GlnfsTer18
ENST00000635849.1:c.2491_2492insAAACACACCCAACA	ENSP00000490948.1:p.Pro831GlnfsTer18
ENST00000635957.1:c.2122_2123insAAACACACCCAACA	ENSP00000490385.1:p.Pro708GlnfsTer18
ENST00000636227.1:n.3633_3634insAAACACACCCAACA
ENST00000636254.1:n.1090_1091insAAACACACCCAACA
ENST00000636930.2:c.5170_5171insAAACACACCCAACA MANE Select	ENSP00000490491.2:p.Pro1724GlnfsTer18
ENST00000636940.1:n.3167_3168insAAACACACCCAACA
ENST00000637015.1:c.2538_2539insAAACACACCCAACA
ENST00000637568.1:c.2452_2453insAAACACACCCAACA
ENST00000637741.1:n.1836_1837insAAACACACCCAACA
ENST00000637810.1:c.2512_2513insAAACACACCCAACA	ENSP00000489636.1:p.Pro838GlnfsTer18
ENST00000637904.1:c.2671_2672insAAACACACCCAACA	ENSP00000490550.1:p.Pro891GlnfsTer18
ENST00000647938.1:c.4801_4802insAAACACACCCAACA	ENSP00000498155.1:p.Pro1601GlnfsTer18
ENST00000346085.9:c.4801_4802insAAACACACCCAACA	ENSP00000344546.4:p.Pro1601GlnfsTer18
ENST00000350026.9:c.4762_4763insAAACACACCCAACA	ENSP00000055163.7:p.Pro1588GlnfsTer18
ENST00000414678.6:c.3328_3329insAAACACACCCAACA	ENSP00000412835.2:p.Pro1110GlnfsTer18
NM_017519.2:c.4762_4763insAAACACACCCAACA	NP_059989.2:p.Pro1588GlnfsTer18
NM_020732.3:c.4801_4802insAAACACACCCAACA	NP_065783.3:p.Pro1601GlnfsTer18
XM_005267069.3:c.4921_4922insAAACACACCCAACA	XP_005267126.2:p.Pro1641GlnfsTer18
XM_011535984.1:c.4000_4001insAAACACACCCAACA	XP_011534286.1:p.Pro1334GlnfsTer18
XM_011535985.1:c.3820_3821insAAACACACCCAACA	XP_011534287.1:p.Pro1274GlnfsTer18
XM_011535986.1:c.3580_3581insAAACACACCCAACA	XP_011534288.1:p.Pro1194GlnfsTer18
XM_011535987.1:c.3199_3200insAAACACACCCAACA	XP_011534289.1:p.Pro1067GlnfsTer18
XM_011535988.1:c.2062_2063insAAACACACCCAACA	XP_011534290.1:p.Pro688GlnfsTer18
NM_001346813.1:c.4921_4922insAAACACACCCAACA	NP_001333742.1:p.Pro1641GlnfsTer18
NM_001363725.1:c.2671_2672insAAACACACCCAACA	NP_001350654.1:p.Pro891GlnfsTer18
XM_011535984.2:c.5131_5132insAAACACACCCAACA	XP_011534286.2:p.Pro1711GlnfsTer18
XM_011535988.3:c.2062_2063insAAACACACCCAACA	XP_011534290.1:p.Pro688GlnfsTer18
XM_017011103.2:c.5032_5033insAAACACACCCAACA	XP_016866592.1:p.Pro1678GlnfsTer18
XM_017011104.1:c.5002_5003insAAACACACCCAACA	XP_016866593.1:p.Pro1668GlnfsTer18
XM_017011105.2:c.4972_4973insAAACACACCCAACA	XP_016866594.1:p.Pro1658GlnfsTer18
XM_017011106.2:c.4843_4844insAAACACACCCAACA	XP_016866595.1:p.Pro1615GlnfsTer18
XM_017011107.2:c.4822_4823insAAACACACCCAACA	XP_016866596.1:p.Pro1608GlnfsTer18
XR_002956289.1:n.5117_5118insAAACACACCCAACA
NM_001363725.2:c.2671_2672insAAACACACCCAACA	NP_001350654.1:p.Pro891GlnfsTer18
NM_001371656.1:c.5050_5051insAAACACACCCAACA	NP_001358585.1:p.Pro1684GlnfsTer18
NM_001374820.1:c.5050_5051insAAACACACCCAACA	NP_001361749.1:p.Pro1684GlnfsTer18
NM_001374828.1:c.5170_5171insAAACACACCCAACA MANE Select	NP_001361757.1:p.Pro1724GlnfsTer18
NM_017519.3:c.5011_5012insAAACACACCCAACA	NP_059989.3:p.Pro1671GlnfsTer18