Canonical Allele Identifier: CA2680895515

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157199010-A-ACACT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157199010_157199011insCACT , CM000668.2:g.157199010_157199011insCACT	GRCh38
NC_000006.11:g.157520144_157520145insCACT , CM000668.1:g.157520144_157520145insCACT	GRCh37
NC_000006.10:g.157561836_157561837insCACT	NCBI36
NG_032093.1:g.426081_426082insCACT
NG_032093.2:g.426081_426082insCACT
NG_066624.1:g.427985_427986insCACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4320+103_4320+104insCACT	ENSP00000055163.8:n.4320+103_4320+104insCACT
ENST00000414678.8:c.4389+103_4389+104insCACT	ENSP00000412835.3:n.4389+103_4389+104insCACT
ENST00000637015.2:c.4608+103_4608+104insCACT	ENSP00000489729.2:n.4608+103_4608+104insCACT
ENST00000346085.10:c.4359+103_4359+104insCACT	ENSP00000344546.5:n.4359+103_4359+104insCACT
ENST00000350026.10:c.4071+103_4071+104insCACT	ENSP00000055163.7:n.4071+103_4071+104insCACT
ENST00000414678.7:c.2637+103_2637+104insCACT	ENSP00000412835.2:n.2637+103_2637+104insCACT
ENST00000635849.1:c.1800+103_1800+104insCACT	ENSP00000490948.1:n.1800+103_1800+104insCACT
ENST00000635957.1:c.1431+103_1431+104insCACT	ENSP00000490385.1:n.1431+103_1431+104insCACT
ENST00000636227.1:n.2942+103_2942+104insCACT
ENST00000636254.1:n.399+103_399+104insCACT
ENST00000636930.2:c.4479+103_4479+104insCACT MANE Select	ENSP00000490491.2:n.4479+103_4479+104insCACT
ENST00000636940.1:n.2476+103_2476+104insCACT
ENST00000637015.1:c.1847+103_1847+104insCACT
ENST00000637568.1:c.1761+103_1761+104insCACT
ENST00000637741.1:n.1145+103_1145+104insCACT
ENST00000637810.1:c.1821+103_1821+104insCACT	ENSP00000489636.1:n.1821+103_1821+104insCACT
ENST00000637904.1:c.1980+103_1980+104insCACT	ENSP00000490550.1:n.1980+103_1980+104insCACT
ENST00000647938.1:c.4110+103_4110+104insCACT	ENSP00000498155.1:n.4110+103_4110+104insCACT
ENST00000346085.9:c.4110+103_4110+104insCACT	ENSP00000344546.4:n.4110+103_4110+104insCACT
ENST00000350026.9:c.4071+103_4071+104insCACT	ENSP00000055163.7:n.4071+103_4071+104insCACT
ENST00000414678.6:c.2637+103_2637+104insCACT	ENSP00000412835.2:n.2637+103_2637+104insCACT
NM_017519.2:c.4071+103_4071+104insCACT	NP_059989.2:n.4071+103_4071+104insCACT
NM_020732.3:c.4110+103_4110+104insCACT	NP_065783.3:n.4110+103_4110+104insCACT
XM_005267069.3:c.4230+103_4230+104insCACT	XP_005267126.2:n.4230+103_4230+104insCACT
XM_011535984.1:c.3309+103_3309+104insCACT	XP_011534286.1:n.3309+103_3309+104insCACT
XM_011535985.1:c.3129+103_3129+104insCACT	XP_011534287.1:n.3129+103_3129+104insCACT
XM_011535986.1:c.2889+103_2889+104insCACT	XP_011534288.1:n.2889+103_2889+104insCACT
XM_011535987.1:c.2508+103_2508+104insCACT	XP_011534289.1:n.2508+103_2508+104insCACT
XM_011535988.1:c.1371+103_1371+104insCACT	XP_011534290.1:n.1371+103_1371+104insCACT
NM_001346813.1:c.4230+103_4230+104insCACT	NP_001333742.1:n.4230+103_4230+104insCACT
NM_001363725.1:c.1980+103_1980+104insCACT	NP_001350654.1:n.1980+103_1980+104insCACT
XM_011535984.2:c.4440+103_4440+104insCACT	XP_011534286.2:n.4440+103_4440+104insCACT
XM_011535988.3:c.1371+103_1371+104insCACT	XP_011534290.1:n.1371+103_1371+104insCACT
XM_017011103.2:c.4341+103_4341+104insCACT	XP_016866592.1:n.4341+103_4341+104insCACT
XM_017011104.1:c.4311+103_4311+104insCACT	XP_016866593.1:n.4311+103_4311+104insCACT
XM_017011105.2:c.4281+103_4281+104insCACT	XP_016866594.1:n.4281+103_4281+104insCACT
XM_017011106.2:c.4152+103_4152+104insCACT	XP_016866595.1:n.4152+103_4152+104insCACT
XM_017011107.2:c.4131+103_4131+104insCACT	XP_016866596.1:n.4131+103_4131+104insCACT
XR_002956289.1:n.4427-1695_4427-1694insCACT
NM_001363725.2:c.1980+103_1980+104insCACT	NP_001350654.1:n.1980+103_1980+104insCACT
NM_001371656.1:c.4359+103_4359+104insCACT	NP_001358585.1:n.4359+103_4359+104insCACT
NM_001374820.1:c.4359+103_4359+104insCACT	NP_001361749.1:n.4359+103_4359+104insCACT
NM_001374828.1:c.4479+103_4479+104insCACT MANE Select	NP_001361757.1:n.4479+103_4479+104insCACT
NM_017519.3:c.4320+103_4320+104insCACT	NP_059989.3:n.4320+103_4320+104insCACT