Canonical Allele Identifier: CA2573320235

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201407del , CM000668.2:g.157201407del	GRCh38
NC_000006.11:g.157522541del , CM000668.1:g.157522541del	GRCh37
NC_000006.10:g.157564233del	NCBI36
NG_032093.1:g.428478del
NG_032093.2:g.428478del
NG_066624.1:g.430382del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5023del	ENSP00000055163.8:p.Glu1675ArgfsTer9
ENST00000414678.8:c.5092del	ENSP00000412835.3:p.Glu1698ArgfsTer9
ENST00000637015.2:c.5311del	ENSP00000489729.2:p.Glu1771ArgfsTer9
ENST00000346085.10:c.5062del	ENSP00000344546.5:p.Glu1688ArgfsTer9
ENST00000350026.10:c.4774del	ENSP00000055163.7:p.Glu1592ArgfsTer9
ENST00000414678.7:c.3340del	ENSP00000412835.2:p.Glu1114ArgfsTer9
ENST00000635849.1:c.2503del	ENSP00000490948.1:p.Glu835ArgfsTer9
ENST00000635957.1:c.2134del	ENSP00000490385.1:p.Glu712ArgfsTer9
ENST00000636227.1:n.3645del
ENST00000636254.1:n.1102del
ENST00000636930.2:c.5182del MANE Select	ENSP00000490491.2:p.Glu1728ArgfsTer9
ENST00000636940.1:n.3179del
ENST00000637015.1:c.2550del
ENST00000637568.1:c.2464del
ENST00000637741.1:n.1848del
ENST00000637810.1:c.2524del	ENSP00000489636.1:p.Glu842ArgfsTer9
ENST00000637904.1:c.2683del	ENSP00000490550.1:p.Glu895ArgfsTer9
ENST00000647938.1:c.4813del	ENSP00000498155.1:p.Glu1605ArgfsTer9
ENST00000346085.9:c.4813del	ENSP00000344546.4:p.Glu1605ArgfsTer9
ENST00000350026.9:c.4774del	ENSP00000055163.7:p.Glu1592ArgfsTer9
ENST00000414678.6:c.3340del	ENSP00000412835.2:p.Glu1114ArgfsTer9
NM_017519.2:c.4774del	NP_059989.2:p.Glu1592ArgfsTer9
NM_020732.3:c.4813del	NP_065783.3:p.Glu1605ArgfsTer9
XM_005267069.3:c.4933del	XP_005267126.2:p.Glu1645ArgfsTer9
XM_011535984.1:c.4012del	XP_011534286.1:p.Glu1338ArgfsTer9
XM_011535985.1:c.3832del	XP_011534287.1:p.Glu1278ArgfsTer9
XM_011535986.1:c.3592del	XP_011534288.1:p.Glu1198ArgfsTer9
XM_011535987.1:c.3211del	XP_011534289.1:p.Glu1071ArgfsTer9
XM_011535988.1:c.2074del	XP_011534290.1:p.Glu692ArgfsTer9
NM_001346813.1:c.4933del	NP_001333742.1:p.Glu1645ArgfsTer9
NM_001363725.1:c.2683del	NP_001350654.1:p.Glu895ArgfsTer9
XM_011535984.2:c.5143del	XP_011534286.2:p.Glu1715ArgfsTer9
XM_011535988.3:c.2074del	XP_011534290.1:p.Glu692ArgfsTer9
XM_017011103.2:c.5044del	XP_016866592.1:p.Glu1682ArgfsTer9
XM_017011104.1:c.5014del	XP_016866593.1:p.Glu1672ArgfsTer9
XM_017011105.2:c.4984del	XP_016866594.1:p.Glu1662ArgfsTer9
XM_017011106.2:c.4855del	XP_016866595.1:p.Glu1619ArgfsTer9
XM_017011107.2:c.4834del	XP_016866596.1:p.Glu1612ArgfsTer9
XR_002956289.1:n.5129del
NM_001363725.2:c.2683del	NP_001350654.1:p.Glu895ArgfsTer9
NM_001371656.1:c.5062del	NP_001358585.1:p.Glu1688ArgfsTer9
NM_001374820.1:c.5062del	NP_001361749.1:p.Glu1688ArgfsTer9
NM_001374828.1:c.5182del MANE Select	NP_001361757.1:p.Glu1728ArgfsTer9
NM_017519.3:c.5023del	NP_059989.3:p.Glu1675ArgfsTer9