Canonical Allele Identifier: CA915944782

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 818000
• ClinVar RCV Id: RCV001009241
• dbSNP Id: rs1583479670

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189701_157189702delinsA , CM000668.2:g.157189701_157189702delinsA	GRCh38
NC_000006.11:g.157510835_157510836delinsA , CM000668.1:g.157510835_157510836delinsA	GRCh37
NC_000006.10:g.157552527_157552528delinsA	NCBI36
NG_032093.1:g.416772_416773delinsA
NG_032093.2:g.416772_416773delinsA
NG_066624.1:g.418676_418677delinsA

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3820_3821delinsA	ENSP00000055163.8:p.Ala1274LysfsTer7
ENST00000414678.8:c.3889_3890delinsA	ENSP00000412835.3:p.Ala1297LysfsTer7
ENST00000637015.2:c.4108_4109delinsA	ENSP00000489729.2:p.Ala1370LysfsTer7
ENST00000346085.10:c.3859_3860delinsA	ENSP00000344546.5:p.Ala1287LysfsTer7
ENST00000350026.10:c.3571_3572delinsA	ENSP00000055163.7:p.Ala1191LysfsTer7
ENST00000414678.7:c.2137_2138delinsA	ENSP00000412835.2:p.Ala713LysfsTer7
ENST00000635849.1:c.1300_1301delinsA	ENSP00000490948.1:p.Ala434LysfsTer7
ENST00000635957.1:c.934_935delinsA	ENSP00000490385.1:p.Ala312LysfsTer7
ENST00000636930.2:c.3979_3980delinsA MANE Select	ENSP00000490491.2:p.Ala1327LysfsTer7
ENST00000636940.1:n.1976_1977delinsA
ENST00000637015.1:c.1347_1348delinsA
ENST00000637568.1:c.1261_1262delinsA
ENST00000637741.1:n.645_646delinsA
ENST00000637810.1:c.1321_1322delinsA	ENSP00000489636.1:p.Ala441LysfsTer7
ENST00000637904.1:c.1480_1481delinsA	ENSP00000490550.1:p.Ala494LysfsTer7
ENST00000647938.1:c.3610_3611delinsA	ENSP00000498155.1:p.Ala1204LysfsTer7
ENST00000346085.9:c.3610_3611delinsA	ENSP00000344546.4:p.Ala1204LysfsTer7
ENST00000350026.9:c.3571_3572delinsA	ENSP00000055163.7:p.Ala1191LysfsTer7
ENST00000414678.6:c.2137_2138delinsA	ENSP00000412835.2:p.Ala713LysfsTer7
NM_017519.2:c.3571_3572delinsA	NP_059989.2:p.Ala1191LysfsTer7
NM_020732.3:c.3610_3611delinsA	NP_065783.3:p.Ala1204LysfsTer7
XM_005267069.3:c.3730_3731delinsA	XP_005267126.2:p.Ala1244LysfsTer7
XM_011535984.1:c.2809_2810delinsA	XP_011534286.1:p.Ala937LysfsTer7
XM_011535985.1:c.2629_2630delinsA	XP_011534287.1:p.Ala877LysfsTer7
XM_011535986.1:c.2389_2390delinsA	XP_011534288.1:p.Ala797LysfsTer7
XM_011535987.1:c.2008_2009delinsA	XP_011534289.1:p.Ala670LysfsTer7
XM_011535988.1:c.871_872delinsA	XP_011534290.1:p.Ala291LysfsTer7
NM_001346813.1:c.3730_3731delinsA	NP_001333742.1:p.Ala1244LysfsTer7
NM_001363725.1:c.1480_1481delinsA	NP_001350654.1:p.Ala494LysfsTer7
XM_011535984.2:c.3940_3941delinsA	XP_011534286.2:p.Ala1314LysfsTer7
XM_011535988.3:c.871_872delinsA	XP_011534290.1:p.Ala291LysfsTer7
XM_017011103.2:c.3841_3842delinsA	XP_016866592.1:p.Ala1281LysfsTer7
XM_017011104.1:c.3811_3812delinsA	XP_016866593.1:p.Ala1271LysfsTer7
XM_017011105.2:c.3781_3782delinsA	XP_016866594.1:p.Ala1261LysfsTer7
XM_017011106.2:c.3652_3653delinsA	XP_016866595.1:p.Ala1218LysfsTer7
XM_017011107.2:c.3631_3632delinsA	XP_016866596.1:p.Ala1211LysfsTer7
XR_002956289.1:n.4023_4024delinsA
NM_001363725.2:c.1480_1481delinsA	NP_001350654.1:p.Ala494LysfsTer7
NM_001371656.1:c.3859_3860delinsA	NP_001358585.1:p.Ala1287LysfsTer7
NM_001374820.1:c.3859_3860delinsA	NP_001361749.1:p.Ala1287LysfsTer7
NM_001374828.1:c.3979_3980delinsA MANE Select	NP_001361757.1:p.Ala1327LysfsTer7
NM_017519.3:c.3820_3821delinsA	NP_059989.3:p.Ala1274LysfsTer7