Canonical Allele Identifier: CA821316175

Gene: ARID1B

Linked Data

• dbSNP Id: rs1399134290
• MyVariant Identifiers: chr6:g.157520172_157520177del (hg19) ; chr6:g.157199038_157199043del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157199039_157199044del , CM000668.2:g.157199039_157199044del	GRCh38
NC_000006.11:g.157520173_157520178del , CM000668.1:g.157520173_157520178del	GRCh37
NC_000006.10:g.157561865_157561870del	NCBI36
NG_032093.1:g.426110_426115del
NG_032093.2:g.426110_426115del
NG_066624.1:g.428014_428019del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4320+132_4320+137del	ENSP00000055163.8:n.4320+132_4320+137del
ENST00000414678.8:c.4389+132_4389+137del	ENSP00000412835.3:n.4389+132_4389+137del
ENST00000637015.2:c.4608+132_4608+137del	ENSP00000489729.2:n.4608+132_4608+137del
ENST00000346085.10:c.4359+132_4359+137del	ENSP00000344546.5:n.4359+132_4359+137del
ENST00000350026.10:c.4071+132_4071+137del	ENSP00000055163.7:n.4071+132_4071+137del
ENST00000414678.7:c.2637+132_2637+137del	ENSP00000412835.2:n.2637+132_2637+137del
ENST00000635849.1:c.1800+132_1800+137del	ENSP00000490948.1:n.1800+132_1800+137del
ENST00000635957.1:c.1431+132_1431+137del	ENSP00000490385.1:n.1431+132_1431+137del
ENST00000636227.1:n.2942+132_2942+137del
ENST00000636254.1:n.399+132_399+137del
ENST00000636930.2:c.4479+132_4479+137del MANE Select	ENSP00000490491.2:n.4479+132_4479+137del
ENST00000636940.1:n.2476+132_2476+137del
ENST00000637015.1:c.1847+132_1847+137del
ENST00000637568.1:c.1761+132_1761+137del
ENST00000637741.1:n.1145+132_1145+137del
ENST00000637810.1:c.1821+132_1821+137del	ENSP00000489636.1:n.1821+132_1821+137del
ENST00000637904.1:c.1980+132_1980+137del	ENSP00000490550.1:n.1980+132_1980+137del
ENST00000647938.1:c.4110+132_4110+137del	ENSP00000498155.1:n.4110+132_4110+137del
ENST00000346085.9:c.4110+132_4110+137del	ENSP00000344546.4:n.4110+132_4110+137del
ENST00000350026.9:c.4071+132_4071+137del	ENSP00000055163.7:n.4071+132_4071+137del
ENST00000414678.6:c.2637+132_2637+137del	ENSP00000412835.2:n.2637+132_2637+137del
NM_017519.2:c.4071+132_4071+137del	NP_059989.2:n.4071+132_4071+137del
NM_020732.3:c.4110+132_4110+137del	NP_065783.3:n.4110+132_4110+137del
XM_005267069.3:c.4230+132_4230+137del	XP_005267126.2:n.4230+132_4230+137del
XM_011535984.1:c.3309+132_3309+137del	XP_011534286.1:n.3309+132_3309+137del
XM_011535985.1:c.3129+132_3129+137del	XP_011534287.1:n.3129+132_3129+137del
XM_011535986.1:c.2889+132_2889+137del	XP_011534288.1:n.2889+132_2889+137del
XM_011535987.1:c.2508+132_2508+137del	XP_011534289.1:n.2508+132_2508+137del
XM_011535988.1:c.1371+132_1371+137del	XP_011534290.1:n.1371+132_1371+137del
NM_001346813.1:c.4230+132_4230+137del	NP_001333742.1:n.4230+132_4230+137del
NM_001363725.1:c.1980+132_1980+137del	NP_001350654.1:n.1980+132_1980+137del
XM_011535984.2:c.4440+132_4440+137del	XP_011534286.2:n.4440+132_4440+137del
XM_011535988.3:c.1371+132_1371+137del	XP_011534290.1:n.1371+132_1371+137del
XM_017011103.2:c.4341+132_4341+137del	XP_016866592.1:n.4341+132_4341+137del
XM_017011104.1:c.4311+132_4311+137del	XP_016866593.1:n.4311+132_4311+137del
XM_017011105.2:c.4281+132_4281+137del	XP_016866594.1:n.4281+132_4281+137del
XM_017011106.2:c.4152+132_4152+137del	XP_016866595.1:n.4152+132_4152+137del
XM_017011107.2:c.4131+132_4131+137del	XP_016866596.1:n.4131+132_4131+137del
XR_002956289.1:n.4427-1666_4427-1661del
NM_001363725.2:c.1980+132_1980+137del	NP_001350654.1:n.1980+132_1980+137del
NM_001371656.1:c.4359+132_4359+137del	NP_001358585.1:n.4359+132_4359+137del
NM_001374820.1:c.4359+132_4359+137del	NP_001361749.1:n.4359+132_4359+137del
NM_001374828.1:c.4479+132_4479+137del MANE Select	NP_001361757.1:n.4479+132_4479+137del
NM_017519.3:c.4320+132_4320+137del	NP_059989.3:n.4320+132_4320+137del