Canonical Allele Identifier: CA915940437

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201364_157201365delinsG , CM000668.2:g.157201364_157201365delinsG	GRCh38
NC_000006.11:g.157522498_157522499delinsG , CM000668.1:g.157522498_157522499delinsG	GRCh37
NC_000006.10:g.157564190_157564191delinsG	NCBI36
NG_032093.1:g.428435_428436delinsG
NG_032093.2:g.428435_428436delinsG
NG_066624.1:g.430339_430340delinsG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4980_4981delinsG	ENSP00000055163.8:p.Gln1661ArgfsTer23
ENST00000414678.8:c.5049_5050delinsG	ENSP00000412835.3:p.Gln1684ArgfsTer23
ENST00000637015.2:c.5268_5269delinsG	ENSP00000489729.2:p.Gln1757ArgfsTer23
ENST00000346085.10:c.5019_5020delinsG	ENSP00000344546.5:p.Gln1674ArgfsTer23
ENST00000350026.10:c.4731_4732delinsG	ENSP00000055163.7:p.Gln1578ArgfsTer23
ENST00000414678.7:c.3297_3298delinsG	ENSP00000412835.2:p.Gln1100ArgfsTer23
ENST00000635849.1:c.2460_2461delinsG	ENSP00000490948.1:p.Gln821ArgfsTer23
ENST00000635957.1:c.2091_2092delinsG	ENSP00000490385.1:p.Gln698ArgfsTer23
ENST00000636227.1:n.3602_3603delinsG
ENST00000636254.1:n.1059_1060delinsG
ENST00000636930.2:c.5139_5140delinsG MANE Select	ENSP00000490491.2:p.Gln1714ArgfsTer23
ENST00000636940.1:n.3136_3137delinsG
ENST00000637015.1:c.2507_2508delinsG
ENST00000637568.1:c.2421_2422delinsG
ENST00000637741.1:n.1805_1806delinsG
ENST00000637810.1:c.2481_2482delinsG	ENSP00000489636.1:p.Gln828ArgfsTer23
ENST00000637904.1:c.2640_2641delinsG	ENSP00000490550.1:p.Gln881ArgfsTer23
ENST00000647938.1:c.4770_4771delinsG	ENSP00000498155.1:p.Gln1591ArgfsTer23
ENST00000346085.9:c.4770_4771delinsG	ENSP00000344546.4:p.Gln1591ArgfsTer23
ENST00000350026.9:c.4731_4732delinsG	ENSP00000055163.7:p.Gln1578ArgfsTer23
ENST00000414678.6:c.3297_3298delinsG	ENSP00000412835.2:p.Gln1100ArgfsTer23
NM_017519.2:c.4731_4732delinsG	NP_059989.2:p.Gln1578ArgfsTer23
NM_020732.3:c.4770_4771delinsG	NP_065783.3:p.Gln1591ArgfsTer23
XM_005267069.3:c.4890_4891delinsG	XP_005267126.2:p.Gln1631ArgfsTer23
XM_011535984.1:c.3969_3970delinsG	XP_011534286.1:p.Gln1324ArgfsTer23
XM_011535985.1:c.3789_3790delinsG	XP_011534287.1:p.Gln1264ArgfsTer23
XM_011535986.1:c.3549_3550delinsG	XP_011534288.1:p.Gln1184ArgfsTer23
XM_011535987.1:c.3168_3169delinsG	XP_011534289.1:p.Gln1057ArgfsTer23
XM_011535988.1:c.2031_2032delinsG	XP_011534290.1:p.Gln678ArgfsTer23
NM_001346813.1:c.4890_4891delinsG	NP_001333742.1:p.Gln1631ArgfsTer23
NM_001363725.1:c.2640_2641delinsG	NP_001350654.1:p.Gln881ArgfsTer23
XM_011535984.2:c.5100_5101delinsG	XP_011534286.2:p.Gln1701ArgfsTer23
XM_011535988.3:c.2031_2032delinsG	XP_011534290.1:p.Gln678ArgfsTer23
XM_017011103.2:c.5001_5002delinsG	XP_016866592.1:p.Gln1668ArgfsTer23
XM_017011104.1:c.4971_4972delinsG	XP_016866593.1:p.Gln1658ArgfsTer23
XM_017011105.2:c.4941_4942delinsG	XP_016866594.1:p.Gln1648ArgfsTer23
XM_017011106.2:c.4812_4813delinsG	XP_016866595.1:p.Gln1605ArgfsTer23
XM_017011107.2:c.4791_4792delinsG	XP_016866596.1:p.Gln1598ArgfsTer23
XR_002956289.1:n.5086_5087delinsG
NM_001363725.2:c.2640_2641delinsG	NP_001350654.1:p.Gln881ArgfsTer23
NM_001371656.1:c.5019_5020delinsG	NP_001358585.1:p.Gln1674ArgfsTer23
NM_001374820.1:c.5019_5020delinsG	NP_001361749.1:p.Gln1674ArgfsTer23
NM_001374828.1:c.5139_5140delinsG MANE Select	NP_001361757.1:p.Gln1714ArgfsTer23
NM_017519.3:c.4980_4981delinsG	NP_059989.3:p.Gln1661ArgfsTer23