Canonical Allele Identifier: CA1675542264

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198938_157198939delinsGT , CM000668.2:g.157198938_157198939delinsGT	GRCh38
NC_000006.11:g.157520072_157520073delinsGT , CM000668.1:g.157520072_157520073delinsGT	GRCh37
NC_000006.10:g.157561764_157561765delinsGT	NCBI36
NG_032093.1:g.426009_426010delinsGT
NG_032093.2:g.426009_426010delinsGT
NG_066624.1:g.427913_427914delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4320+31_4320+32delinsGT	ENSP00000055163.8:n.4320+31_4320+32delinsGT
ENST00000414678.8:c.4389+31_4389+32delinsGT	ENSP00000412835.3:n.4389+31_4389+32delinsGT
ENST00000637015.2:c.4608+31_4608+32delinsGT	ENSP00000489729.2:n.4608+31_4608+32delinsGT
ENST00000346085.10:c.4359+31_4359+32delinsGT	ENSP00000344546.5:n.4359+31_4359+32delinsGT
ENST00000350026.10:c.4071+31_4071+32delinsGT	ENSP00000055163.7:n.4071+31_4071+32delinsGT
ENST00000414678.7:c.2637+31_2637+32delinsGT	ENSP00000412835.2:n.2637+31_2637+32delinsGT
ENST00000635849.1:c.1800+31_1800+32delinsGT	ENSP00000490948.1:n.1800+31_1800+32delinsGT
ENST00000635957.1:c.1431+31_1431+32delinsGT	ENSP00000490385.1:n.1431+31_1431+32delinsGT
ENST00000636227.1:n.2942+31_2942+32delinsGT
ENST00000636254.1:n.399+31_399+32delinsGT
ENST00000636930.2:c.4479+31_4479+32delinsGT MANE Select	ENSP00000490491.2:n.4479+31_4479+32delinsGT
ENST00000636940.1:n.2476+31_2476+32delinsGT
ENST00000637015.1:c.1847+31_1847+32delinsGT
ENST00000637568.1:c.1761+31_1761+32delinsGT
ENST00000637741.1:n.1145+31_1145+32delinsGT
ENST00000637810.1:c.1821+31_1821+32delinsGT	ENSP00000489636.1:n.1821+31_1821+32delinsGT
ENST00000637904.1:c.1980+31_1980+32delinsGT	ENSP00000490550.1:n.1980+31_1980+32delinsGT
ENST00000647938.1:c.4110+31_4110+32delinsGT	ENSP00000498155.1:n.4110+31_4110+32delinsGT
ENST00000346085.9:c.4110+31_4110+32delinsGT	ENSP00000344546.4:n.4110+31_4110+32delinsGT
ENST00000350026.9:c.4071+31_4071+32delinsGT	ENSP00000055163.7:n.4071+31_4071+32delinsGT
ENST00000414678.6:c.2637+31_2637+32delinsGT	ENSP00000412835.2:n.2637+31_2637+32delinsGT
NM_017519.2:c.4071+31_4071+32delinsGT	NP_059989.2:n.4071+31_4071+32delinsGT
NM_020732.3:c.4110+31_4110+32delinsGT	NP_065783.3:n.4110+31_4110+32delinsGT
XM_005267069.3:c.4230+31_4230+32delinsGT	XP_005267126.2:n.4230+31_4230+32delinsGT
XM_011535984.1:c.3309+31_3309+32delinsGT	XP_011534286.1:n.3309+31_3309+32delinsGT
XM_011535985.1:c.3129+31_3129+32delinsGT	XP_011534287.1:n.3129+31_3129+32delinsGT
XM_011535986.1:c.2889+31_2889+32delinsGT	XP_011534288.1:n.2889+31_2889+32delinsGT
XM_011535987.1:c.2508+31_2508+32delinsGT	XP_011534289.1:n.2508+31_2508+32delinsGT
XM_011535988.1:c.1371+31_1371+32delinsGT	XP_011534290.1:n.1371+31_1371+32delinsGT
NM_001346813.1:c.4230+31_4230+32delinsGT	NP_001333742.1:n.4230+31_4230+32delinsGT
NM_001363725.1:c.1980+31_1980+32delinsGT	NP_001350654.1:n.1980+31_1980+32delinsGT
XM_011535984.2:c.4440+31_4440+32delinsGT	XP_011534286.2:n.4440+31_4440+32delinsGT
XM_011535988.3:c.1371+31_1371+32delinsGT	XP_011534290.1:n.1371+31_1371+32delinsGT
XM_017011103.2:c.4341+31_4341+32delinsGT	XP_016866592.1:n.4341+31_4341+32delinsGT
XM_017011104.1:c.4311+31_4311+32delinsGT	XP_016866593.1:n.4311+31_4311+32delinsGT
XM_017011105.2:c.4281+31_4281+32delinsGT	XP_016866594.1:n.4281+31_4281+32delinsGT
XM_017011106.2:c.4152+31_4152+32delinsGT	XP_016866595.1:n.4152+31_4152+32delinsGT
XM_017011107.2:c.4131+31_4131+32delinsGT	XP_016866596.1:n.4131+31_4131+32delinsGT
XR_002956289.1:n.4427-1767_4427-1766delinsGT
NM_001363725.2:c.1980+31_1980+32delinsGT	NP_001350654.1:n.1980+31_1980+32delinsGT
NM_001371656.1:c.4359+31_4359+32delinsGT	NP_001358585.1:n.4359+31_4359+32delinsGT
NM_001374820.1:c.4359+31_4359+32delinsGT	NP_001361749.1:n.4359+31_4359+32delinsGT
NM_001374828.1:c.4479+31_4479+32delinsGT MANE Select	NP_001361757.1:n.4479+31_4479+32delinsGT
NM_017519.3:c.4320+31_4320+32delinsGT	NP_059989.3:n.4320+31_4320+32delinsGT