Canonical Allele Identifier: CA1675542339
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157199116_157199117delinsGA , CM000668.2:g.157199116_157199117delinsGA GRCh38
NC_000006.11:g.157520250_157520251delinsGA , CM000668.1:g.157520250_157520251delinsGA GRCh37
NC_000006.10:g.157561942_157561943delinsGA NCBI36
NG_032093.1:g.426187_426188delinsGA
NG_032093.2:g.426187_426188delinsGA
NG_066624.1:g.428091_428092delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4320+209_4320+210delinsGA ENSP00000055163.8:n.4320+209_4320+210delinsGA
ENST00000414678.8:c.4389+209_4389+210delinsGA ENSP00000412835.3:n.4389+209_4389+210delinsGA
ENST00000637015.2:c.4608+209_4608+210delinsGA ENSP00000489729.2:n.4608+209_4608+210delinsGA
ENST00000346085.10:c.4359+209_4359+210delinsGA ENSP00000344546.5:n.4359+209_4359+210delinsGA
ENST00000350026.10:c.4071+209_4071+210delinsGA ENSP00000055163.7:n.4071+209_4071+210delinsGA
ENST00000414678.7:c.2637+209_2637+210delinsGA ENSP00000412835.2:n.2637+209_2637+210delinsGA
ENST00000635849.1:c.1800+209_1800+210delinsGA ENSP00000490948.1:n.1800+209_1800+210delinsGA
ENST00000635957.1:c.1431+209_1431+210delinsGA ENSP00000490385.1:n.1431+209_1431+210delinsGA
ENST00000636227.1:n.2942+209_2942+210delinsGA
ENST00000636254.1:n.399+209_399+210delinsGA
ENST00000636930.2:c.4479+209_4479+210delinsGA MANE Select ENSP00000490491.2:n.4479+209_4479+210delinsGA
ENST00000636940.1:n.2476+209_2476+210delinsGA
ENST00000637015.1:c.1847+209_1847+210delinsGA
ENST00000637568.1:c.1761+209_1761+210delinsGA
ENST00000637741.1:n.1145+209_1145+210delinsGA
ENST00000637810.1:c.1821+209_1821+210delinsGA ENSP00000489636.1:n.1821+209_1821+210delinsGA
ENST00000637904.1:c.1980+209_1980+210delinsGA ENSP00000490550.1:n.1980+209_1980+210delinsGA
ENST00000647938.1:c.4110+209_4110+210delinsGA ENSP00000498155.1:n.4110+209_4110+210delinsGA
ENST00000346085.9:c.4110+209_4110+210delinsGA ENSP00000344546.4:n.4110+209_4110+210delinsGA
ENST00000350026.9:c.4071+209_4071+210delinsGA ENSP00000055163.7:n.4071+209_4071+210delinsGA
ENST00000414678.6:c.2637+209_2637+210delinsGA ENSP00000412835.2:n.2637+209_2637+210delinsGA
NM_017519.2:c.4071+209_4071+210delinsGA NP_059989.2:n.4071+209_4071+210delinsGA
NM_020732.3:c.4110+209_4110+210delinsGA NP_065783.3:n.4110+209_4110+210delinsGA
XM_005267069.3:c.4230+209_4230+210delinsGA XP_005267126.2:n.4230+209_4230+210delinsGA
XM_011535984.1:c.3309+209_3309+210delinsGA XP_011534286.1:n.3309+209_3309+210delinsGA
XM_011535985.1:c.3129+209_3129+210delinsGA XP_011534287.1:n.3129+209_3129+210delinsGA
XM_011535986.1:c.2889+209_2889+210delinsGA XP_011534288.1:n.2889+209_2889+210delinsGA
XM_011535987.1:c.2508+209_2508+210delinsGA XP_011534289.1:n.2508+209_2508+210delinsGA
XM_011535988.1:c.1371+209_1371+210delinsGA XP_011534290.1:n.1371+209_1371+210delinsGA
NM_001346813.1:c.4230+209_4230+210delinsGA NP_001333742.1:n.4230+209_4230+210delinsGA
NM_001363725.1:c.1980+209_1980+210delinsGA NP_001350654.1:n.1980+209_1980+210delinsGA
XM_011535984.2:c.4440+209_4440+210delinsGA XP_011534286.2:n.4440+209_4440+210delinsGA
XM_011535988.3:c.1371+209_1371+210delinsGA XP_011534290.1:n.1371+209_1371+210delinsGA
XM_017011103.2:c.4341+209_4341+210delinsGA XP_016866592.1:n.4341+209_4341+210delinsGA
XM_017011104.1:c.4311+209_4311+210delinsGA XP_016866593.1:n.4311+209_4311+210delinsGA
XM_017011105.2:c.4281+209_4281+210delinsGA XP_016866594.1:n.4281+209_4281+210delinsGA
XM_017011106.2:c.4152+209_4152+210delinsGA XP_016866595.1:n.4152+209_4152+210delinsGA
XM_017011107.2:c.4131+209_4131+210delinsGA XP_016866596.1:n.4131+209_4131+210delinsGA
XR_002956289.1:n.4427-1589_4427-1588delinsGA
NM_001363725.2:c.1980+209_1980+210delinsGA NP_001350654.1:n.1980+209_1980+210delinsGA
NM_001371656.1:c.4359+209_4359+210delinsGA NP_001358585.1:n.4359+209_4359+210delinsGA
NM_001374820.1:c.4359+209_4359+210delinsGA NP_001361749.1:n.4359+209_4359+210delinsGA
NM_001374828.1:c.4479+209_4479+210delinsGA MANE Select NP_001361757.1:n.4479+209_4479+210delinsGA
NM_017519.3:c.4320+209_4320+210delinsGA NP_059989.3:n.4320+209_4320+210delinsGA