Canonical Allele Identifier: CA2680895551

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157199043-A-AGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157199044_157199045insCTG , CM000668.2:g.157199044_157199045insCTG	GRCh38
NC_000006.11:g.157520178_157520179insCTG , CM000668.1:g.157520178_157520179insCTG	GRCh37
NC_000006.10:g.157561870_157561871insCTG	NCBI36
NG_032093.1:g.426115_426116insCTG
NG_032093.2:g.426115_426116insCTG
NG_066624.1:g.428019_428020insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4320+137_4320+138insCTG	ENSP00000055163.8:n.4320+137_4320+138insCTG
ENST00000414678.8:c.4389+137_4389+138insCTG	ENSP00000412835.3:n.4389+137_4389+138insCTG
ENST00000637015.2:c.4608+137_4608+138insCTG	ENSP00000489729.2:n.4608+137_4608+138insCTG
ENST00000346085.10:c.4359+137_4359+138insCTG	ENSP00000344546.5:n.4359+137_4359+138insCTG
ENST00000350026.10:c.4071+137_4071+138insCTG	ENSP00000055163.7:n.4071+137_4071+138insCTG
ENST00000414678.7:c.2637+137_2637+138insCTG	ENSP00000412835.2:n.2637+137_2637+138insCTG
ENST00000635849.1:c.1800+137_1800+138insCTG	ENSP00000490948.1:n.1800+137_1800+138insCTG
ENST00000635957.1:c.1431+137_1431+138insCTG	ENSP00000490385.1:n.1431+137_1431+138insCTG
ENST00000636227.1:n.2942+137_2942+138insCTG
ENST00000636254.1:n.399+137_399+138insCTG
ENST00000636930.2:c.4479+137_4479+138insCTG MANE Select	ENSP00000490491.2:n.4479+137_4479+138insCTG
ENST00000636940.1:n.2476+137_2476+138insCTG
ENST00000637015.1:c.1847+137_1847+138insCTG
ENST00000637568.1:c.1761+137_1761+138insCTG
ENST00000637741.1:n.1145+137_1145+138insCTG
ENST00000637810.1:c.1821+137_1821+138insCTG	ENSP00000489636.1:n.1821+137_1821+138insCTG
ENST00000637904.1:c.1980+137_1980+138insCTG	ENSP00000490550.1:n.1980+137_1980+138insCTG
ENST00000647938.1:c.4110+137_4110+138insCTG	ENSP00000498155.1:n.4110+137_4110+138insCTG
ENST00000346085.9:c.4110+137_4110+138insCTG	ENSP00000344546.4:n.4110+137_4110+138insCTG
ENST00000350026.9:c.4071+137_4071+138insCTG	ENSP00000055163.7:n.4071+137_4071+138insCTG
ENST00000414678.6:c.2637+137_2637+138insCTG	ENSP00000412835.2:n.2637+137_2637+138insCTG
NM_017519.2:c.4071+137_4071+138insCTG	NP_059989.2:n.4071+137_4071+138insCTG
NM_020732.3:c.4110+137_4110+138insCTG	NP_065783.3:n.4110+137_4110+138insCTG
XM_005267069.3:c.4230+137_4230+138insCTG	XP_005267126.2:n.4230+137_4230+138insCTG
XM_011535984.1:c.3309+137_3309+138insCTG	XP_011534286.1:n.3309+137_3309+138insCTG
XM_011535985.1:c.3129+137_3129+138insCTG	XP_011534287.1:n.3129+137_3129+138insCTG
XM_011535986.1:c.2889+137_2889+138insCTG	XP_011534288.1:n.2889+137_2889+138insCTG
XM_011535987.1:c.2508+137_2508+138insCTG	XP_011534289.1:n.2508+137_2508+138insCTG
XM_011535988.1:c.1371+137_1371+138insCTG	XP_011534290.1:n.1371+137_1371+138insCTG
NM_001346813.1:c.4230+137_4230+138insCTG	NP_001333742.1:n.4230+137_4230+138insCTG
NM_001363725.1:c.1980+137_1980+138insCTG	NP_001350654.1:n.1980+137_1980+138insCTG
XM_011535984.2:c.4440+137_4440+138insCTG	XP_011534286.2:n.4440+137_4440+138insCTG
XM_011535988.3:c.1371+137_1371+138insCTG	XP_011534290.1:n.1371+137_1371+138insCTG
XM_017011103.2:c.4341+137_4341+138insCTG	XP_016866592.1:n.4341+137_4341+138insCTG
XM_017011104.1:c.4311+137_4311+138insCTG	XP_016866593.1:n.4311+137_4311+138insCTG
XM_017011105.2:c.4281+137_4281+138insCTG	XP_016866594.1:n.4281+137_4281+138insCTG
XM_017011106.2:c.4152+137_4152+138insCTG	XP_016866595.1:n.4152+137_4152+138insCTG
XM_017011107.2:c.4131+137_4131+138insCTG	XP_016866596.1:n.4131+137_4131+138insCTG
XR_002956289.1:n.4427-1661_4427-1660insCTG
NM_001363725.2:c.1980+137_1980+138insCTG	NP_001350654.1:n.1980+137_1980+138insCTG
NM_001371656.1:c.4359+137_4359+138insCTG	NP_001358585.1:n.4359+137_4359+138insCTG
NM_001374820.1:c.4359+137_4359+138insCTG	NP_001361749.1:n.4359+137_4359+138insCTG
NM_001374828.1:c.4479+137_4479+138insCTG MANE Select	NP_001361757.1:n.4479+137_4479+138insCTG
NM_017519.3:c.4320+137_4320+138insCTG	NP_059989.3:n.4320+137_4320+138insCTG