Canonical Allele Identifier: CA1675538246

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189700_157189702delinsGGC , CM000668.2:g.157189700_157189702delinsGGC	GRCh38
NC_000006.11:g.157510834_157510836delinsGGC , CM000668.1:g.157510834_157510836delinsGGC	GRCh37
NC_000006.10:g.157552526_157552528delinsGGC	NCBI36
NG_032093.1:g.416771_416773delinsGGC
NG_032093.2:g.416771_416773delinsGGC
NG_066624.1:g.418675_418677delinsGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3819_3821delinsGGC	ENSP00000055163.8:p.Met1273=
ENST00000414678.8:c.3888_3890delinsGGC	ENSP00000412835.3:p.Met1296=
ENST00000637015.2:c.4107_4109delinsGGC	ENSP00000489729.2:p.Met1369=
ENST00000346085.10:c.3858_3860delinsGGC	ENSP00000344546.5:p.Met1286=
ENST00000350026.10:c.3570_3572delinsGGC	ENSP00000055163.7:p.Met1190=
ENST00000414678.7:c.2136_2138delinsGGC	ENSP00000412835.2:p.Met712=
ENST00000635849.1:c.1299_1301delinsGGC	ENSP00000490948.1:p.Met433=
ENST00000635957.1:c.933_935delinsGGC	ENSP00000490385.1:p.Met311=
ENST00000636930.2:c.3978_3980delinsGGC MANE Select	ENSP00000490491.2:p.Met1326=
ENST00000636940.1:n.1975_1977delinsGGC
ENST00000637015.1:c.1346_1348delinsGGC
ENST00000637568.1:c.1260_1262delinsGGC
ENST00000637741.1:n.644_646delinsGGC
ENST00000637810.1:c.1320_1322delinsGGC	ENSP00000489636.1:p.Met440=
ENST00000637904.1:c.1479_1481delinsGGC	ENSP00000490550.1:p.Met493=
ENST00000647938.1:c.3609_3611delinsGGC	ENSP00000498155.1:p.Met1203=
ENST00000346085.9:c.3609_3611delinsGGC	ENSP00000344546.4:p.Met1203=
ENST00000350026.9:c.3570_3572delinsGGC	ENSP00000055163.7:p.Met1190=
ENST00000414678.6:c.2136_2138delinsGGC	ENSP00000412835.2:p.Met712=
NM_017519.2:c.3570_3572delinsGGC	NP_059989.2:p.Met1190=
NM_020732.3:c.3609_3611delinsGGC	NP_065783.3:p.Met1203=
XM_005267069.3:c.3729_3731delinsGGC	XP_005267126.2:p.Met1243=
XM_011535984.1:c.2808_2810delinsGGC	XP_011534286.1:p.Met936=
XM_011535985.1:c.2628_2630delinsGGC	XP_011534287.1:p.Met876=
XM_011535986.1:c.2388_2390delinsGGC	XP_011534288.1:p.Met796=
XM_011535987.1:c.2007_2009delinsGGC	XP_011534289.1:p.Met669=
XM_011535988.1:c.870_872delinsGGC	XP_011534290.1:p.Met290=
NM_001346813.1:c.3729_3731delinsGGC	NP_001333742.1:p.Met1243=
NM_001363725.1:c.1479_1481delinsGGC	NP_001350654.1:p.Met493=
XM_011535984.2:c.3939_3941delinsGGC	XP_011534286.2:p.Met1313=
XM_011535988.3:c.870_872delinsGGC	XP_011534290.1:p.Met290=
XM_017011103.2:c.3840_3842delinsGGC	XP_016866592.1:p.Met1280=
XM_017011104.1:c.3810_3812delinsGGC	XP_016866593.1:p.Met1270=
XM_017011105.2:c.3780_3782delinsGGC	XP_016866594.1:p.Met1260=
XM_017011106.2:c.3651_3653delinsGGC	XP_016866595.1:p.Met1217=
XM_017011107.2:c.3630_3632delinsGGC	XP_016866596.1:p.Met1210=
XR_002956289.1:n.4022_4024delinsGGC
NM_001363725.2:c.1479_1481delinsGGC	NP_001350654.1:p.Met493=
NM_001371656.1:c.3858_3860delinsGGC	NP_001358585.1:p.Met1286=
NM_001374820.1:c.3858_3860delinsGGC	NP_001361749.1:p.Met1286=
NM_001374828.1:c.3978_3980delinsGGC MANE Select	NP_001361757.1:p.Met1326=
NM_017519.3:c.3819_3821delinsGGC	NP_059989.3:p.Met1273=