Canonical Allele Identifier: CA1675523383

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201317C= , CM000668.2:g.157201317C=	GRCh38
NC_000006.11:g.157522451C= , CM000668.1:g.157522451C=	GRCh37
NC_000006.10:g.157564143C=	NCBI36
NG_032093.1:g.428388C=
NG_032093.2:g.428388C=
NG_066624.1:g.430292C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4933C=	ENSP00000055163.8:p.Leu1645=
ENST00000414678.8:c.5002C=	ENSP00000412835.3:p.Leu1668=
ENST00000637015.2:c.5221C=	ENSP00000489729.2:p.Leu1741=
ENST00000346085.10:c.4972C=	ENSP00000344546.5:p.Leu1658=
ENST00000350026.10:c.4684C=	ENSP00000055163.7:p.Leu1562=
ENST00000414678.7:c.3250C=	ENSP00000412835.2:p.Leu1084=
ENST00000635849.1:c.2413C=	ENSP00000490948.1:p.Leu805=
ENST00000635957.1:c.2044C=	ENSP00000490385.1:p.Leu682=
ENST00000636227.1:n.3555C=
ENST00000636254.1:n.1012C=
ENST00000636930.2:c.5092C= MANE Select	ENSP00000490491.2:p.Leu1698=
ENST00000636940.1:n.3089C=
ENST00000637015.1:c.2460C=
ENST00000637568.1:c.2374C=
ENST00000637741.1:n.1758C=
ENST00000637810.1:c.2434C=	ENSP00000489636.1:p.Leu812=
ENST00000637904.1:c.2593C=	ENSP00000490550.1:p.Leu865=
ENST00000647938.1:c.4723C=	ENSP00000498155.1:p.Leu1575=
ENST00000346085.9:c.4723C=	ENSP00000344546.4:p.Leu1575=
ENST00000350026.9:c.4684C=	ENSP00000055163.7:p.Leu1562=
ENST00000414678.6:c.3250C=	ENSP00000412835.2:p.Leu1084=
NM_017519.2:c.4684C=	NP_059989.2:p.Leu1562=
NM_020732.3:c.4723C=	NP_065783.3:p.Leu1575=
XM_005267069.3:c.4843C=	XP_005267126.2:p.Leu1615=
XM_011535984.1:c.3922C=	XP_011534286.1:p.Leu1308=
XM_011535985.1:c.3742C=	XP_011534287.1:p.Leu1248=
XM_011535986.1:c.3502C=	XP_011534288.1:p.Leu1168=
XM_011535987.1:c.3121C=	XP_011534289.1:p.Leu1041=
XM_011535988.1:c.1984C=	XP_011534290.1:p.Leu662=
NM_001346813.1:c.4843C=	NP_001333742.1:p.Leu1615=
NM_001363725.1:c.2593C=	NP_001350654.1:p.Leu865=
XM_011535984.2:c.5053C=	XP_011534286.2:p.Leu1685=
XM_011535988.3:c.1984C=	XP_011534290.1:p.Leu662=
XM_017011103.2:c.4954C=	XP_016866592.1:p.Leu1652=
XM_017011104.1:c.4924C=	XP_016866593.1:p.Leu1642=
XM_017011105.2:c.4894C=	XP_016866594.1:p.Leu1632=
XM_017011106.2:c.4765C=	XP_016866595.1:p.Leu1589=
XM_017011107.2:c.4744C=	XP_016866596.1:p.Leu1582=
XR_002956289.1:n.5039C=
NM_001363725.2:c.2593C=	NP_001350654.1:p.Leu865=
NM_001371656.1:c.4972C=	NP_001358585.1:p.Leu1658=
NM_001374820.1:c.4972C=	NP_001361749.1:p.Leu1658=
NM_001374828.1:c.5092C= MANE Select	NP_001361757.1:p.Leu1698=
NM_017519.3:c.4933C=	NP_059989.3:p.Leu1645=