Canonical Allele Identifier: CA1675542324

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157199074_157199075delinsGA , CM000668.2:g.157199074_157199075delinsGA	GRCh38
NC_000006.11:g.157520208_157520209delinsGA , CM000668.1:g.157520208_157520209delinsGA	GRCh37
NC_000006.10:g.157561900_157561901delinsGA	NCBI36
NG_032093.1:g.426145_426146delinsGA
NG_032093.2:g.426145_426146delinsGA
NG_066624.1:g.428049_428050delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4320+167_4320+168delinsGA	ENSP00000055163.8:n.4320+167_4320+168delinsGA
ENST00000414678.8:c.4389+167_4389+168delinsGA	ENSP00000412835.3:n.4389+167_4389+168delinsGA
ENST00000637015.2:c.4608+167_4608+168delinsGA	ENSP00000489729.2:n.4608+167_4608+168delinsGA
ENST00000346085.10:c.4359+167_4359+168delinsGA	ENSP00000344546.5:n.4359+167_4359+168delinsGA
ENST00000350026.10:c.4071+167_4071+168delinsGA	ENSP00000055163.7:n.4071+167_4071+168delinsGA
ENST00000414678.7:c.2637+167_2637+168delinsGA	ENSP00000412835.2:n.2637+167_2637+168delinsGA
ENST00000635849.1:c.1800+167_1800+168delinsGA	ENSP00000490948.1:n.1800+167_1800+168delinsGA
ENST00000635957.1:c.1431+167_1431+168delinsGA	ENSP00000490385.1:n.1431+167_1431+168delinsGA
ENST00000636227.1:n.2942+167_2942+168delinsGA
ENST00000636254.1:n.399+167_399+168delinsGA
ENST00000636930.2:c.4479+167_4479+168delinsGA MANE Select	ENSP00000490491.2:n.4479+167_4479+168delinsGA
ENST00000636940.1:n.2476+167_2476+168delinsGA
ENST00000637015.1:c.1847+167_1847+168delinsGA
ENST00000637568.1:c.1761+167_1761+168delinsGA
ENST00000637741.1:n.1145+167_1145+168delinsGA
ENST00000637810.1:c.1821+167_1821+168delinsGA	ENSP00000489636.1:n.1821+167_1821+168delinsGA
ENST00000637904.1:c.1980+167_1980+168delinsGA	ENSP00000490550.1:n.1980+167_1980+168delinsGA
ENST00000647938.1:c.4110+167_4110+168delinsGA	ENSP00000498155.1:n.4110+167_4110+168delinsGA
ENST00000346085.9:c.4110+167_4110+168delinsGA	ENSP00000344546.4:n.4110+167_4110+168delinsGA
ENST00000350026.9:c.4071+167_4071+168delinsGA	ENSP00000055163.7:n.4071+167_4071+168delinsGA
ENST00000414678.6:c.2637+167_2637+168delinsGA	ENSP00000412835.2:n.2637+167_2637+168delinsGA
NM_017519.2:c.4071+167_4071+168delinsGA	NP_059989.2:n.4071+167_4071+168delinsGA
NM_020732.3:c.4110+167_4110+168delinsGA	NP_065783.3:n.4110+167_4110+168delinsGA
XM_005267069.3:c.4230+167_4230+168delinsGA	XP_005267126.2:n.4230+167_4230+168delinsGA
XM_011535984.1:c.3309+167_3309+168delinsGA	XP_011534286.1:n.3309+167_3309+168delinsGA
XM_011535985.1:c.3129+167_3129+168delinsGA	XP_011534287.1:n.3129+167_3129+168delinsGA
XM_011535986.1:c.2889+167_2889+168delinsGA	XP_011534288.1:n.2889+167_2889+168delinsGA
XM_011535987.1:c.2508+167_2508+168delinsGA	XP_011534289.1:n.2508+167_2508+168delinsGA
XM_011535988.1:c.1371+167_1371+168delinsGA	XP_011534290.1:n.1371+167_1371+168delinsGA
NM_001346813.1:c.4230+167_4230+168delinsGA	NP_001333742.1:n.4230+167_4230+168delinsGA
NM_001363725.1:c.1980+167_1980+168delinsGA	NP_001350654.1:n.1980+167_1980+168delinsGA
XM_011535984.2:c.4440+167_4440+168delinsGA	XP_011534286.2:n.4440+167_4440+168delinsGA
XM_011535988.3:c.1371+167_1371+168delinsGA	XP_011534290.1:n.1371+167_1371+168delinsGA
XM_017011103.2:c.4341+167_4341+168delinsGA	XP_016866592.1:n.4341+167_4341+168delinsGA
XM_017011104.1:c.4311+167_4311+168delinsGA	XP_016866593.1:n.4311+167_4311+168delinsGA
XM_017011105.2:c.4281+167_4281+168delinsGA	XP_016866594.1:n.4281+167_4281+168delinsGA
XM_017011106.2:c.4152+167_4152+168delinsGA	XP_016866595.1:n.4152+167_4152+168delinsGA
XM_017011107.2:c.4131+167_4131+168delinsGA	XP_016866596.1:n.4131+167_4131+168delinsGA
XR_002956289.1:n.4427-1631_4427-1630delinsGA
NM_001363725.2:c.1980+167_1980+168delinsGA	NP_001350654.1:n.1980+167_1980+168delinsGA
NM_001371656.1:c.4359+167_4359+168delinsGA	NP_001358585.1:n.4359+167_4359+168delinsGA
NM_001374820.1:c.4359+167_4359+168delinsGA	NP_001361749.1:n.4359+167_4359+168delinsGA
NM_001374828.1:c.4479+167_4479+168delinsGA MANE Select	NP_001361757.1:n.4479+167_4479+168delinsGA
NM_017519.3:c.4320+167_4320+168delinsGA	NP_059989.3:n.4320+167_4320+168delinsGA