Canonical Allele Identifier: CA1675523036

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201131_157201134delinsCCTT , CM000668.2:g.157201131_157201134delinsCCTT	GRCh38
NC_000006.11:g.157522265_157522268delinsCCTT , CM000668.1:g.157522265_157522268delinsCCTT	GRCh37
NC_000006.10:g.157563957_157563960delinsCCTT	NCBI36
NG_032093.1:g.428202_428205delinsCCTT
NG_032093.2:g.428202_428205delinsCCTT
NG_066624.1:g.430106_430109delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4747_4750delinsCCTT	ENSP00000055163.8:p.Pro1583=
ENST00000414678.8:c.4816_4819delinsCCTT	ENSP00000412835.3:p.Pro1606=
ENST00000637015.2:c.5035_5038delinsCCTT	ENSP00000489729.2:p.Pro1679=
ENST00000346085.10:c.4786_4789delinsCCTT	ENSP00000344546.5:p.Pro1596=
ENST00000350026.10:c.4498_4501delinsCCTT	ENSP00000055163.7:p.Pro1500=
ENST00000414678.7:c.3064_3067delinsCCTT	ENSP00000412835.2:p.Pro1022=
ENST00000635849.1:c.2227_2230delinsCCTT	ENSP00000490948.1:p.Pro743=
ENST00000635957.1:c.1858_1861delinsCCTT	ENSP00000490385.1:p.Pro620=
ENST00000636227.1:n.3369_3372delinsCCTT
ENST00000636254.1:n.826_829delinsCCTT
ENST00000636930.2:c.4906_4909delinsCCTT MANE Select	ENSP00000490491.2:p.Pro1636=
ENST00000636940.1:n.2903_2906delinsCCTT
ENST00000637015.1:c.2274_2277delinsCCTT
ENST00000637568.1:c.2188_2191delinsCCTT
ENST00000637741.1:n.1572_1575delinsCCTT
ENST00000637810.1:c.2248_2251delinsCCTT	ENSP00000489636.1:p.Pro750=
ENST00000637904.1:c.2407_2410delinsCCTT	ENSP00000490550.1:p.Pro803=
ENST00000647938.1:c.4537_4540delinsCCTT	ENSP00000498155.1:p.Pro1513=
ENST00000346085.9:c.4537_4540delinsCCTT	ENSP00000344546.4:p.Pro1513=
ENST00000350026.9:c.4498_4501delinsCCTT	ENSP00000055163.7:p.Pro1500=
ENST00000414678.6:c.3064_3067delinsCCTT	ENSP00000412835.2:p.Pro1022=
NM_017519.2:c.4498_4501delinsCCTT	NP_059989.2:p.Pro1500=
NM_020732.3:c.4537_4540delinsCCTT	NP_065783.3:p.Pro1513=
XM_005267069.3:c.4657_4660delinsCCTT	XP_005267126.2:p.Pro1553=
XM_011535984.1:c.3736_3739delinsCCTT	XP_011534286.1:p.Pro1246=
XM_011535985.1:c.3556_3559delinsCCTT	XP_011534287.1:p.Pro1186=
XM_011535986.1:c.3316_3319delinsCCTT	XP_011534288.1:p.Pro1106=
XM_011535987.1:c.2935_2938delinsCCTT	XP_011534289.1:p.Pro979=
XM_011535988.1:c.1798_1801delinsCCTT	XP_011534290.1:p.Pro600=
NM_001346813.1:c.4657_4660delinsCCTT	NP_001333742.1:p.Pro1553=
NM_001363725.1:c.2407_2410delinsCCTT	NP_001350654.1:p.Pro803=
XM_011535984.2:c.4867_4870delinsCCTT	XP_011534286.2:p.Pro1623=
XM_011535988.3:c.1798_1801delinsCCTT	XP_011534290.1:p.Pro600=
XM_017011103.2:c.4768_4771delinsCCTT	XP_016866592.1:p.Pro1590=
XM_017011104.1:c.4738_4741delinsCCTT	XP_016866593.1:p.Pro1580=
XM_017011105.2:c.4708_4711delinsCCTT	XP_016866594.1:p.Pro1570=
XM_017011106.2:c.4579_4582delinsCCTT	XP_016866595.1:p.Pro1527=
XM_017011107.2:c.4558_4561delinsCCTT	XP_016866596.1:p.Pro1520=
XR_002956289.1:n.4853_4856delinsCCTT
NM_001363725.2:c.2407_2410delinsCCTT	NP_001350654.1:p.Pro803=
NM_001371656.1:c.4786_4789delinsCCTT	NP_001358585.1:p.Pro1596=
NM_001374820.1:c.4786_4789delinsCCTT	NP_001361749.1:p.Pro1596=
NM_001374828.1:c.4906_4909delinsCCTT MANE Select	NP_001361757.1:p.Pro1636=
NM_017519.3:c.4747_4750delinsCCTT	NP_059989.3:p.Pro1583=