Canonical Allele Identifier: CA2680895561

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157199052-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157199052_157199053insC , CM000668.2:g.157199052_157199053insC	GRCh38
NC_000006.11:g.157520186_157520187insC , CM000668.1:g.157520186_157520187insC	GRCh37
NC_000006.10:g.157561878_157561879insC	NCBI36
NG_032093.1:g.426123_426124insC
NG_032093.2:g.426123_426124insC
NG_066624.1:g.428027_428028insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4320+145_4320+146insC	ENSP00000055163.8:n.4320+145_4320+146insC
ENST00000414678.8:c.4389+145_4389+146insC	ENSP00000412835.3:n.4389+145_4389+146insC
ENST00000637015.2:c.4608+145_4608+146insC	ENSP00000489729.2:n.4608+145_4608+146insC
ENST00000346085.10:c.4359+145_4359+146insC	ENSP00000344546.5:n.4359+145_4359+146insC
ENST00000350026.10:c.4071+145_4071+146insC	ENSP00000055163.7:n.4071+145_4071+146insC
ENST00000414678.7:c.2637+145_2637+146insC	ENSP00000412835.2:n.2637+145_2637+146insC
ENST00000635849.1:c.1800+145_1800+146insC	ENSP00000490948.1:n.1800+145_1800+146insC
ENST00000635957.1:c.1431+145_1431+146insC	ENSP00000490385.1:n.1431+145_1431+146insC
ENST00000636227.1:n.2942+145_2942+146insC
ENST00000636254.1:n.399+145_399+146insC
ENST00000636930.2:c.4479+145_4479+146insC MANE Select	ENSP00000490491.2:n.4479+145_4479+146insC
ENST00000636940.1:n.2476+145_2476+146insC
ENST00000637015.1:c.1847+145_1847+146insC
ENST00000637568.1:c.1761+145_1761+146insC
ENST00000637741.1:n.1145+145_1145+146insC
ENST00000637810.1:c.1821+145_1821+146insC	ENSP00000489636.1:n.1821+145_1821+146insC
ENST00000637904.1:c.1980+145_1980+146insC	ENSP00000490550.1:n.1980+145_1980+146insC
ENST00000647938.1:c.4110+145_4110+146insC	ENSP00000498155.1:n.4110+145_4110+146insC
ENST00000346085.9:c.4110+145_4110+146insC	ENSP00000344546.4:n.4110+145_4110+146insC
ENST00000350026.9:c.4071+145_4071+146insC	ENSP00000055163.7:n.4071+145_4071+146insC
ENST00000414678.6:c.2637+145_2637+146insC	ENSP00000412835.2:n.2637+145_2637+146insC
NM_017519.2:c.4071+145_4071+146insC	NP_059989.2:n.4071+145_4071+146insC
NM_020732.3:c.4110+145_4110+146insC	NP_065783.3:n.4110+145_4110+146insC
XM_005267069.3:c.4230+145_4230+146insC	XP_005267126.2:n.4230+145_4230+146insC
XM_011535984.1:c.3309+145_3309+146insC	XP_011534286.1:n.3309+145_3309+146insC
XM_011535985.1:c.3129+145_3129+146insC	XP_011534287.1:n.3129+145_3129+146insC
XM_011535986.1:c.2889+145_2889+146insC	XP_011534288.1:n.2889+145_2889+146insC
XM_011535987.1:c.2508+145_2508+146insC	XP_011534289.1:n.2508+145_2508+146insC
XM_011535988.1:c.1371+145_1371+146insC	XP_011534290.1:n.1371+145_1371+146insC
NM_001346813.1:c.4230+145_4230+146insC	NP_001333742.1:n.4230+145_4230+146insC
NM_001363725.1:c.1980+145_1980+146insC	NP_001350654.1:n.1980+145_1980+146insC
XM_011535984.2:c.4440+145_4440+146insC	XP_011534286.2:n.4440+145_4440+146insC
XM_011535988.3:c.1371+145_1371+146insC	XP_011534290.1:n.1371+145_1371+146insC
XM_017011103.2:c.4341+145_4341+146insC	XP_016866592.1:n.4341+145_4341+146insC
XM_017011104.1:c.4311+145_4311+146insC	XP_016866593.1:n.4311+145_4311+146insC
XM_017011105.2:c.4281+145_4281+146insC	XP_016866594.1:n.4281+145_4281+146insC
XM_017011106.2:c.4152+145_4152+146insC	XP_016866595.1:n.4152+145_4152+146insC
XM_017011107.2:c.4131+145_4131+146insC	XP_016866596.1:n.4131+145_4131+146insC
XR_002956289.1:n.4427-1653_4427-1652insC
NM_001363725.2:c.1980+145_1980+146insC	NP_001350654.1:n.1980+145_1980+146insC
NM_001371656.1:c.4359+145_4359+146insC	NP_001358585.1:n.4359+145_4359+146insC
NM_001374820.1:c.4359+145_4359+146insC	NP_001361749.1:n.4359+145_4359+146insC
NM_001374828.1:c.4479+145_4479+146insC MANE Select	NP_001361757.1:n.4479+145_4479+146insC
NM_017519.3:c.4320+145_4320+146insC	NP_059989.3:n.4320+145_4320+146insC