Canonical Allele Identifier: CA1675542320

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157199070_157199071delinsTG , CM000668.2:g.157199070_157199071delinsTG	GRCh38
NC_000006.11:g.157520204_157520205delinsTG , CM000668.1:g.157520204_157520205delinsTG	GRCh37
NC_000006.10:g.157561896_157561897delinsTG	NCBI36
NG_032093.1:g.426141_426142delinsTG
NG_032093.2:g.426141_426142delinsTG
NG_066624.1:g.428045_428046delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4320+163_4320+164delinsTG	ENSP00000055163.8:n.4320+163_4320+164delinsTG
ENST00000414678.8:c.4389+163_4389+164delinsTG	ENSP00000412835.3:n.4389+163_4389+164delinsTG
ENST00000637015.2:c.4608+163_4608+164delinsTG	ENSP00000489729.2:n.4608+163_4608+164delinsTG
ENST00000346085.10:c.4359+163_4359+164delinsTG	ENSP00000344546.5:n.4359+163_4359+164delinsTG
ENST00000350026.10:c.4071+163_4071+164delinsTG	ENSP00000055163.7:n.4071+163_4071+164delinsTG
ENST00000414678.7:c.2637+163_2637+164delinsTG	ENSP00000412835.2:n.2637+163_2637+164delinsTG
ENST00000635849.1:c.1800+163_1800+164delinsTG	ENSP00000490948.1:n.1800+163_1800+164delinsTG
ENST00000635957.1:c.1431+163_1431+164delinsTG	ENSP00000490385.1:n.1431+163_1431+164delinsTG
ENST00000636227.1:n.2942+163_2942+164delinsTG
ENST00000636254.1:n.399+163_399+164delinsTG
ENST00000636930.2:c.4479+163_4479+164delinsTG MANE Select	ENSP00000490491.2:n.4479+163_4479+164delinsTG
ENST00000636940.1:n.2476+163_2476+164delinsTG
ENST00000637015.1:c.1847+163_1847+164delinsTG
ENST00000637568.1:c.1761+163_1761+164delinsTG
ENST00000637741.1:n.1145+163_1145+164delinsTG
ENST00000637810.1:c.1821+163_1821+164delinsTG	ENSP00000489636.1:n.1821+163_1821+164delinsTG
ENST00000637904.1:c.1980+163_1980+164delinsTG	ENSP00000490550.1:n.1980+163_1980+164delinsTG
ENST00000647938.1:c.4110+163_4110+164delinsTG	ENSP00000498155.1:n.4110+163_4110+164delinsTG
ENST00000346085.9:c.4110+163_4110+164delinsTG	ENSP00000344546.4:n.4110+163_4110+164delinsTG
ENST00000350026.9:c.4071+163_4071+164delinsTG	ENSP00000055163.7:n.4071+163_4071+164delinsTG
ENST00000414678.6:c.2637+163_2637+164delinsTG	ENSP00000412835.2:n.2637+163_2637+164delinsTG
NM_017519.2:c.4071+163_4071+164delinsTG	NP_059989.2:n.4071+163_4071+164delinsTG
NM_020732.3:c.4110+163_4110+164delinsTG	NP_065783.3:n.4110+163_4110+164delinsTG
XM_005267069.3:c.4230+163_4230+164delinsTG	XP_005267126.2:n.4230+163_4230+164delinsTG
XM_011535984.1:c.3309+163_3309+164delinsTG	XP_011534286.1:n.3309+163_3309+164delinsTG
XM_011535985.1:c.3129+163_3129+164delinsTG	XP_011534287.1:n.3129+163_3129+164delinsTG
XM_011535986.1:c.2889+163_2889+164delinsTG	XP_011534288.1:n.2889+163_2889+164delinsTG
XM_011535987.1:c.2508+163_2508+164delinsTG	XP_011534289.1:n.2508+163_2508+164delinsTG
XM_011535988.1:c.1371+163_1371+164delinsTG	XP_011534290.1:n.1371+163_1371+164delinsTG
NM_001346813.1:c.4230+163_4230+164delinsTG	NP_001333742.1:n.4230+163_4230+164delinsTG
NM_001363725.1:c.1980+163_1980+164delinsTG	NP_001350654.1:n.1980+163_1980+164delinsTG
XM_011535984.2:c.4440+163_4440+164delinsTG	XP_011534286.2:n.4440+163_4440+164delinsTG
XM_011535988.3:c.1371+163_1371+164delinsTG	XP_011534290.1:n.1371+163_1371+164delinsTG
XM_017011103.2:c.4341+163_4341+164delinsTG	XP_016866592.1:n.4341+163_4341+164delinsTG
XM_017011104.1:c.4311+163_4311+164delinsTG	XP_016866593.1:n.4311+163_4311+164delinsTG
XM_017011105.2:c.4281+163_4281+164delinsTG	XP_016866594.1:n.4281+163_4281+164delinsTG
XM_017011106.2:c.4152+163_4152+164delinsTG	XP_016866595.1:n.4152+163_4152+164delinsTG
XM_017011107.2:c.4131+163_4131+164delinsTG	XP_016866596.1:n.4131+163_4131+164delinsTG
XR_002956289.1:n.4427-1635_4427-1634delinsTG
NM_001363725.2:c.1980+163_1980+164delinsTG	NP_001350654.1:n.1980+163_1980+164delinsTG
NM_001371656.1:c.4359+163_4359+164delinsTG	NP_001358585.1:n.4359+163_4359+164delinsTG
NM_001374820.1:c.4359+163_4359+164delinsTG	NP_001361749.1:n.4359+163_4359+164delinsTG
NM_001374828.1:c.4479+163_4479+164delinsTG MANE Select	NP_001361757.1:n.4479+163_4479+164delinsTG
NM_017519.3:c.4320+163_4320+164delinsTG	NP_059989.3:n.4320+163_4320+164delinsTG