Canonical Allele Identifier: CA2695207245

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181125_157181126insA , CM000668.2:g.157181125_157181126insA	GRCh38
NC_000006.11:g.157502259_157502260insA , CM000668.1:g.157502259_157502260insA	GRCh37
NC_000006.10:g.157543951_157543952insA	NCBI36
NG_032093.1:g.408196_408197insA
NG_032093.2:g.408196_408197insA
NG_066624.1:g.410100_410101insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3502_3503insA	ENSP00000055163.8:p.Leu1168HisfsTer20
ENST00000414678.8:c.3571_3572insA	ENSP00000412835.3:p.Leu1191HisfsTer20
ENST00000637015.2:c.3790_3791insA	ENSP00000489729.2:p.Leu1264HisfsTer20
ENST00000319584.11:c.1675_1676insA	ENSP00000313006.7:p.Leu559HisfsTer20
ENST00000346085.10:c.3541_3542insA	ENSP00000344546.5:p.Leu1181HisfsTer20
ENST00000350026.10:c.3253_3254insA	ENSP00000055163.7:p.Leu1085HisfsTer20
ENST00000414678.7:c.1819_1820insA	ENSP00000412835.2:p.Leu607HisfsTer20
ENST00000635849.1:c.982_983insA	ENSP00000490948.1:p.Leu328HisfsTer20
ENST00000635957.1:c.616_617insA	ENSP00000490385.1:p.Leu206HisfsTer20
ENST00000636930.2:c.3661_3662insA MANE Select	ENSP00000490491.2:p.Leu1221HisfsTer20
ENST00000636940.1:n.1658_1659insA
ENST00000637015.1:c.1029_1030insA
ENST00000637568.1:c.943_944insA
ENST00000637741.1:n.327_328insA
ENST00000637810.1:c.1003_1004insA	ENSP00000489636.1:p.Leu335HisfsTer20
ENST00000637904.1:c.1162_1163insA	ENSP00000490550.1:p.Leu388HisfsTer20
ENST00000647938.1:c.3292_3293insA	ENSP00000498155.1:p.Leu1098HisfsTer20
ENST00000319584.10:c.1678_1679insA	ENSP00000313006.6:p.Leu560HisfsTer20
ENST00000346085.9:c.3292_3293insA	ENSP00000344546.4:p.Leu1098HisfsTer20
ENST00000350026.9:c.3253_3254insA	ENSP00000055163.7:p.Leu1085HisfsTer20
ENST00000400790.3:c.454_455insA	ENSP00000383596.3:p.Leu152HisfsTer20
ENST00000414678.6:c.1819_1820insA	ENSP00000412835.2:p.Leu607HisfsTer20
ENST00000478761.3:c.863_864insA
NM_017519.2:c.3253_3254insA	NP_059989.2:p.Leu1085HisfsTer20
NM_020732.3:c.3292_3293insA	NP_065783.3:p.Leu1098HisfsTer20
XM_005267069.3:c.3412_3413insA	XP_005267126.2:p.Leu1138HisfsTer20
XM_011535984.1:c.2491_2492insA	XP_011534286.1:p.Leu831HisfsTer20
XM_011535985.1:c.2311_2312insA	XP_011534287.1:p.Leu771HisfsTer20
XM_011535986.1:c.2071_2072insA	XP_011534288.1:p.Leu691HisfsTer20
XM_011535987.1:c.1690_1691insA	XP_011534289.1:p.Leu564HisfsTer20
XM_011535988.1:c.553_554insA	XP_011534290.1:p.Leu185HisfsTer20
NM_001346813.1:c.3412_3413insA	NP_001333742.1:p.Leu1138HisfsTer20
NM_001363725.1:c.1162_1163insA	NP_001350654.1:p.Leu388HisfsTer20
XM_011535984.2:c.3622_3623insA	XP_011534286.2:p.Leu1208HisfsTer20
XM_011535988.3:c.553_554insA	XP_011534290.1:p.Leu185HisfsTer20
XM_017011103.2:c.3523_3524insA	XP_016866592.1:p.Leu1175HisfsTer20
XM_017011104.1:c.3493_3494insA	XP_016866593.1:p.Leu1165HisfsTer20
XM_017011105.2:c.3463_3464insA	XP_016866594.1:p.Leu1155HisfsTer20
XM_017011106.2:c.3334_3335insA	XP_016866595.1:p.Leu1112HisfsTer20
XM_017011107.2:c.3313_3314insA	XP_016866596.1:p.Leu1105HisfsTer20
XR_002956289.1:n.3705_3706insA
NM_001363725.2:c.1162_1163insA	NP_001350654.1:p.Leu388HisfsTer20
NM_001371656.1:c.3541_3542insA	NP_001358585.1:p.Leu1181HisfsTer20
NM_001374820.1:c.3541_3542insA	NP_001361749.1:p.Leu1181HisfsTer20
NM_001374828.1:c.3661_3662insA MANE Select	NP_001361757.1:p.Leu1221HisfsTer20
NM_017519.3:c.3502_3503insA	NP_059989.3:p.Leu1168HisfsTer20