Canonical Allele Identifier: CA2573052632

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207149dup , CM000668.2:g.157207149dup	GRCh38
NC_000006.11:g.157528283dup , CM000668.1:g.157528283dup	GRCh37
NC_000006.10:g.157569975dup	NCBI36
NG_032093.1:g.434220dup
NG_032093.2:g.434220dup
NG_066624.1:g.436124dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.6218dup	ENSP00000055163.8:p.Val2075GlyfsTer7
ENST00000414678.8:c.6287dup	ENSP00000412835.3:p.Val2098GlyfsTer7
ENST00000637015.2:c.6506dup	ENSP00000489729.2:p.Val2171GlyfsTer7
ENST00000346085.10:c.6257dup	ENSP00000344546.5:p.Val2088GlyfsTer7
ENST00000350026.10:c.5969dup	ENSP00000055163.7:p.Val1992GlyfsTer7
ENST00000414678.7:c.4535dup	ENSP00000412835.2:p.Val1514GlyfsTer7
ENST00000635849.1:c.3698dup	ENSP00000490948.1:p.Val1235GlyfsTer7
ENST00000635928.1:c.533dup	ENSP00000489717.1:p.Val180GlyfsTer7
ENST00000635957.1:c.3329dup	ENSP00000490385.1:p.Val1112GlyfsTer7
ENST00000636227.1:n.4840dup
ENST00000636254.1:n.2297dup
ENST00000636930.2:c.6377dup MANE Select	ENSP00000490491.2:p.Val2128GlyfsTer7
ENST00000636940.1:n.4374dup
ENST00000637015.1:c.3745dup
ENST00000637568.1:c.3659dup
ENST00000637741.1:n.3043dup
ENST00000637810.1:c.3719dup	ENSP00000489636.1:p.Val1242GlyfsTer7
ENST00000637904.1:c.3878dup	ENSP00000490550.1:p.Val1295GlyfsTer7
ENST00000637933.1:n.3492dup
ENST00000647938.1:c.6008dup	ENSP00000498155.1:p.Val2005GlyfsTer7
ENST00000346085.9:c.6008dup	ENSP00000344546.4:p.Val2005GlyfsTer7
ENST00000350026.9:c.5969dup	ENSP00000055163.7:p.Val1992GlyfsTer7
ENST00000414678.6:c.4535dup	ENSP00000412835.2:p.Val1514GlyfsTer7
NM_017519.2:c.5969dup	NP_059989.2:p.Val1992GlyfsTer7
NM_020732.3:c.6008dup	NP_065783.3:p.Val2005GlyfsTer7
XM_005267069.3:c.6128dup	XP_005267126.2:p.Val2045GlyfsTer7
XM_011535984.1:c.5207dup	XP_011534286.1:p.Val1738GlyfsTer7
XM_011535985.1:c.5027dup	XP_011534287.1:p.Val1678GlyfsTer7
XM_011535986.1:c.4787dup	XP_011534288.1:p.Val1598GlyfsTer7
XM_011535987.1:c.4406dup	XP_011534289.1:p.Val1471GlyfsTer7
XM_011535988.1:c.3269dup	XP_011534290.1:p.Val1092GlyfsTer7
NM_001346813.1:c.6128dup	NP_001333742.1:p.Val2045GlyfsTer7
NM_001363725.1:c.3878dup	NP_001350654.1:p.Val1295GlyfsTer7
XM_011535984.2:c.6338dup	XP_011534286.2:p.Val2115GlyfsTer7
XM_011535988.3:c.3269dup	XP_011534290.1:p.Val1092GlyfsTer7
XM_017011103.2:c.6239dup	XP_016866592.1:p.Val2082GlyfsTer7
XM_017011104.1:c.6209dup	XP_016866593.1:p.Val2072GlyfsTer7
XM_017011105.2:c.6179dup	XP_016866594.1:p.Val2062GlyfsTer7
XM_017011106.2:c.6050dup	XP_016866595.1:p.Val2019GlyfsTer7
XM_017011107.2:c.6029dup	XP_016866596.1:p.Val2012GlyfsTer7
XR_002956289.1:n.6324dup
NM_001363725.2:c.3878dup	NP_001350654.1:p.Val1295GlyfsTer7
NM_001371656.1:c.6257dup	NP_001358585.1:p.Val2088GlyfsTer7
NM_001374820.1:c.6257dup	NP_001361749.1:p.Val2088GlyfsTer7
NM_001374828.1:c.6377dup MANE Select	NP_001361757.1:p.Val2128GlyfsTer7
NM_017519.3:c.6218dup	NP_059989.3:p.Val2075GlyfsTer7