Canonical Allele Identifier: CA2739289480

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201387_157201388insC , CM000668.2:g.157201387_157201388insC	GRCh38
NC_000006.11:g.157522521_157522522insC , CM000668.1:g.157522521_157522522insC	GRCh37
NC_000006.10:g.157564213_157564214insC	NCBI36
NG_032093.1:g.428458_428459insC
NG_032093.2:g.428458_428459insC
NG_066624.1:g.430362_430363insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5003_5004insC	ENSP00000055163.8:p.Gln1668HisfsTer?
ENST00000414678.8:c.5072_5073insC	ENSP00000412835.3:p.Gln1691HisfsTer?
ENST00000637015.2:c.5291_5292insC	ENSP00000489729.2:p.Gln1764HisfsTer?
ENST00000346085.10:c.5042_5043insC	ENSP00000344546.5:p.Gln1681HisfsTer?
ENST00000350026.10:c.4754_4755insC	ENSP00000055163.7:p.Gln1585HisfsTer?
ENST00000414678.7:c.3320_3321insC	ENSP00000412835.2:p.Gln1107HisfsTer?
ENST00000635849.1:c.2483_2484insC	ENSP00000490948.1:p.Gln828HisfsTer?
ENST00000635957.1:c.2114_2115insC	ENSP00000490385.1:p.Gln705HisfsTer?
ENST00000636227.1:n.3625_3626insC
ENST00000636254.1:n.1082_1083insC
ENST00000636930.2:c.5162_5163insC MANE Select	ENSP00000490491.2:p.Gln1721HisfsTer?
ENST00000636940.1:n.3159_3160insC
ENST00000637015.1:c.2530_2531insC
ENST00000637568.1:c.2444_2445insC
ENST00000637741.1:n.1828_1829insC
ENST00000637810.1:c.2504_2505insC	ENSP00000489636.1:p.Gln835HisfsTer?
ENST00000637904.1:c.2663_2664insC	ENSP00000490550.1:p.Gln888HisfsTer?
ENST00000647938.1:c.4793_4794insC	ENSP00000498155.1:p.Gln1598HisfsTer?
ENST00000346085.9:c.4793_4794insC	ENSP00000344546.4:p.Gln1598HisfsTer?
ENST00000350026.9:c.4754_4755insC	ENSP00000055163.7:p.Gln1585HisfsTer?
ENST00000414678.6:c.3320_3321insC	ENSP00000412835.2:p.Gln1107HisfsTer?
NM_017519.2:c.4754_4755insC	NP_059989.2:p.Gln1585HisfsTer?
NM_020732.3:c.4793_4794insC	NP_065783.3:p.Gln1598HisfsTer?
XM_005267069.3:c.4913_4914insC	XP_005267126.2:p.Gln1638HisfsTer?
XM_011535984.1:c.3992_3993insC	XP_011534286.1:p.Gln1331HisfsTer?
XM_011535985.1:c.3812_3813insC	XP_011534287.1:p.Gln1271HisfsTer?
XM_011535986.1:c.3572_3573insC	XP_011534288.1:p.Gln1191HisfsTer?
XM_011535987.1:c.3191_3192insC	XP_011534289.1:p.Gln1064HisfsTer?
XM_011535988.1:c.2054_2055insC	XP_011534290.1:p.Gln685HisfsTer?
NM_001346813.1:c.4913_4914insC	NP_001333742.1:p.Gln1638HisfsTer?
NM_001363725.1:c.2663_2664insC	NP_001350654.1:p.Gln888HisfsTer?
XM_011535984.2:c.5123_5124insC	XP_011534286.2:p.Gln1708HisfsTer?
XM_011535988.3:c.2054_2055insC	XP_011534290.1:p.Gln685HisfsTer?
XM_017011103.2:c.5024_5025insC	XP_016866592.1:p.Gln1675HisfsTer?
XM_017011104.1:c.4994_4995insC	XP_016866593.1:p.Gln1665HisfsTer?
XM_017011105.2:c.4964_4965insC	XP_016866594.1:p.Gln1655HisfsTer?
XM_017011106.2:c.4835_4836insC	XP_016866595.1:p.Gln1612HisfsTer?
XM_017011107.2:c.4814_4815insC	XP_016866596.1:p.Gln1605HisfsTer?
XR_002956289.1:n.5109_5110insC
NM_001363725.2:c.2663_2664insC	NP_001350654.1:p.Gln888HisfsTer?
NM_001371656.1:c.5042_5043insC	NP_001358585.1:p.Gln1681HisfsTer?
NM_001374820.1:c.5042_5043insC	NP_001361749.1:p.Gln1681HisfsTer?
NM_001374828.1:c.5162_5163insC MANE Select	NP_001361757.1:p.Gln1721HisfsTer?
NM_017519.3:c.5003_5004insC	NP_059989.3:p.Gln1668HisfsTer?