Canonical Allele Identifier: CA2739289479

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201378dup , CM000668.2:g.157201378dup	GRCh38
NC_000006.11:g.157522512dup , CM000668.1:g.157522512dup	GRCh37
NC_000006.10:g.157564204dup	NCBI36
NG_032093.1:g.428449dup
NG_032093.2:g.428449dup
NG_066624.1:g.430353dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4994dup	ENSP00000055163.8:p.Pro1666ThrfsTer?
ENST00000414678.8:c.5063dup	ENSP00000412835.3:p.Pro1689ThrfsTer?
ENST00000637015.2:c.5282dup	ENSP00000489729.2:p.Pro1762ThrfsTer?
ENST00000346085.10:c.5033dup	ENSP00000344546.5:p.Pro1679ThrfsTer?
ENST00000350026.10:c.4745dup	ENSP00000055163.7:p.Pro1583ThrfsTer?
ENST00000414678.7:c.3311dup	ENSP00000412835.2:p.Pro1105ThrfsTer?
ENST00000635849.1:c.2474dup	ENSP00000490948.1:p.Pro826ThrfsTer?
ENST00000635957.1:c.2105dup	ENSP00000490385.1:p.Pro703ThrfsTer?
ENST00000636227.1:n.3616dup
ENST00000636254.1:n.1073dup
ENST00000636930.2:c.5153dup MANE Select	ENSP00000490491.2:p.Pro1719ThrfsTer?
ENST00000636940.1:n.3150dup
ENST00000637015.1:c.2521dup
ENST00000637568.1:c.2435dup
ENST00000637741.1:n.1819dup
ENST00000637810.1:c.2495dup	ENSP00000489636.1:p.Pro833ThrfsTer?
ENST00000637904.1:c.2654dup	ENSP00000490550.1:p.Pro886ThrfsTer?
ENST00000647938.1:c.4784dup	ENSP00000498155.1:p.Pro1596ThrfsTer?
ENST00000346085.9:c.4784dup	ENSP00000344546.4:p.Pro1596ThrfsTer?
ENST00000350026.9:c.4745dup	ENSP00000055163.7:p.Pro1583ThrfsTer?
ENST00000414678.6:c.3311dup	ENSP00000412835.2:p.Pro1105ThrfsTer?
NM_017519.2:c.4745dup	NP_059989.2:p.Pro1583ThrfsTer?
NM_020732.3:c.4784dup	NP_065783.3:p.Pro1596ThrfsTer?
XM_005267069.3:c.4904dup	XP_005267126.2:p.Pro1636ThrfsTer?
XM_011535984.1:c.3983dup	XP_011534286.1:p.Pro1329ThrfsTer?
XM_011535985.1:c.3803dup	XP_011534287.1:p.Pro1269ThrfsTer?
XM_011535986.1:c.3563dup	XP_011534288.1:p.Pro1189ThrfsTer?
XM_011535987.1:c.3182dup	XP_011534289.1:p.Pro1062ThrfsTer?
XM_011535988.1:c.2045dup	XP_011534290.1:p.Pro683ThrfsTer?
NM_001346813.1:c.4904dup	NP_001333742.1:p.Pro1636ThrfsTer?
NM_001363725.1:c.2654dup	NP_001350654.1:p.Pro886ThrfsTer?
XM_011535984.2:c.5114dup	XP_011534286.2:p.Pro1706ThrfsTer?
XM_011535988.3:c.2045dup	XP_011534290.1:p.Pro683ThrfsTer?
XM_017011103.2:c.5015dup	XP_016866592.1:p.Pro1673ThrfsTer?
XM_017011104.1:c.4985dup	XP_016866593.1:p.Pro1663ThrfsTer?
XM_017011105.2:c.4955dup	XP_016866594.1:p.Pro1653ThrfsTer?
XM_017011106.2:c.4826dup	XP_016866595.1:p.Pro1610ThrfsTer?
XM_017011107.2:c.4805dup	XP_016866596.1:p.Pro1603ThrfsTer?
XR_002956289.1:n.5100dup
NM_001363725.2:c.2654dup	NP_001350654.1:p.Pro886ThrfsTer?
NM_001371656.1:c.5033dup	NP_001358585.1:p.Pro1679ThrfsTer?
NM_001374820.1:c.5033dup	NP_001361749.1:p.Pro1679ThrfsTer?
NM_001374828.1:c.5153dup MANE Select	NP_001361757.1:p.Pro1719ThrfsTer?
NM_017519.3:c.4994dup	NP_059989.3:p.Pro1666ThrfsTer?