Canonical Allele Identifier: CA1675538242

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189686_157189688delinsGGC , CM000668.2:g.157189686_157189688delinsGGC	GRCh38
NC_000006.11:g.157510820_157510822delinsGGC , CM000668.1:g.157510820_157510822delinsGGC	GRCh37
NC_000006.10:g.157552512_157552514delinsGGC	NCBI36
NG_032093.1:g.416757_416759delinsGGC
NG_032093.2:g.416757_416759delinsGGC
NG_066624.1:g.418661_418663delinsGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3805_3807delinsGGC	ENSP00000055163.8:p.Gly1269=
ENST00000414678.8:c.3874_3876delinsGGC	ENSP00000412835.3:p.Gly1292=
ENST00000637015.2:c.4093_4095delinsGGC	ENSP00000489729.2:p.Gly1365=
ENST00000346085.10:c.3844_3846delinsGGC	ENSP00000344546.5:p.Gly1282=
ENST00000350026.10:c.3556_3558delinsGGC	ENSP00000055163.7:p.Gly1186=
ENST00000414678.7:c.2122_2124delinsGGC	ENSP00000412835.2:p.Gly708=
ENST00000635849.1:c.1285_1287delinsGGC	ENSP00000490948.1:p.Gly429=
ENST00000635957.1:c.919_921delinsGGC	ENSP00000490385.1:p.Gly307=
ENST00000636930.2:c.3964_3966delinsGGC MANE Select	ENSP00000490491.2:p.Gly1322=
ENST00000636940.1:n.1961_1963delinsGGC
ENST00000637015.1:c.1332_1334delinsGGC
ENST00000637568.1:c.1246_1248delinsGGC
ENST00000637741.1:n.630_632delinsGGC
ENST00000637810.1:c.1306_1308delinsGGC	ENSP00000489636.1:p.Gly436=
ENST00000637904.1:c.1465_1467delinsGGC	ENSP00000490550.1:p.Gly489=
ENST00000647938.1:c.3595_3597delinsGGC	ENSP00000498155.1:p.Gly1199=
ENST00000346085.9:c.3595_3597delinsGGC	ENSP00000344546.4:p.Gly1199=
ENST00000350026.9:c.3556_3558delinsGGC	ENSP00000055163.7:p.Gly1186=
ENST00000414678.6:c.2122_2124delinsGGC	ENSP00000412835.2:p.Gly708=
NM_017519.2:c.3556_3558delinsGGC	NP_059989.2:p.Gly1186=
NM_020732.3:c.3595_3597delinsGGC	NP_065783.3:p.Gly1199=
XM_005267069.3:c.3715_3717delinsGGC	XP_005267126.2:p.Gly1239=
XM_011535984.1:c.2794_2796delinsGGC	XP_011534286.1:p.Gly932=
XM_011535985.1:c.2614_2616delinsGGC	XP_011534287.1:p.Gly872=
XM_011535986.1:c.2374_2376delinsGGC	XP_011534288.1:p.Gly792=
XM_011535987.1:c.1993_1995delinsGGC	XP_011534289.1:p.Gly665=
XM_011535988.1:c.856_858delinsGGC	XP_011534290.1:p.Gly286=
NM_001346813.1:c.3715_3717delinsGGC	NP_001333742.1:p.Gly1239=
NM_001363725.1:c.1465_1467delinsGGC	NP_001350654.1:p.Gly489=
XM_011535984.2:c.3925_3927delinsGGC	XP_011534286.2:p.Gly1309=
XM_011535988.3:c.856_858delinsGGC	XP_011534290.1:p.Gly286=
XM_017011103.2:c.3826_3828delinsGGC	XP_016866592.1:p.Gly1276=
XM_017011104.1:c.3796_3798delinsGGC	XP_016866593.1:p.Gly1266=
XM_017011105.2:c.3766_3768delinsGGC	XP_016866594.1:p.Gly1256=
XM_017011106.2:c.3637_3639delinsGGC	XP_016866595.1:p.Gly1213=
XM_017011107.2:c.3616_3618delinsGGC	XP_016866596.1:p.Gly1206=
XR_002956289.1:n.4008_4010delinsGGC
NM_001363725.2:c.1465_1467delinsGGC	NP_001350654.1:p.Gly489=
NM_001371656.1:c.3844_3846delinsGGC	NP_001358585.1:p.Gly1282=
NM_001374820.1:c.3844_3846delinsGGC	NP_001361749.1:p.Gly1282=
NM_001374828.1:c.3964_3966delinsGGC MANE Select	NP_001361757.1:p.Gly1322=
NM_017519.3:c.3805_3807delinsGGC	NP_059989.3:p.Gly1269=