Canonical Allele Identifier: CA2773707692

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148881_157148882insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC , CM000668.2:g.157148881_157148882insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	GRCh38
NC_000006.11:g.157470015_157470016insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC , CM000668.1:g.157470015_157470016insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	GRCh37
NC_000006.10:g.157511707_157511708insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	NCBI36
NG_032093.1:g.375952_375953insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC
NG_032093.2:g.375952_375953insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC
NG_066624.1:g.377856_377857insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3019_3020insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000055163.8:p.Thr1007ArgfsTer2
ENST00000414678.8:c.2929_2930insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000412835.3:p.Thr977ArgfsTer2
ENST00000637015.2:c.3019_3020insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000489729.2:p.Thr1007ArgfsTer2
ENST00000319584.11:c.1033_1034insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000313006.7:p.Thr345ArgfsTer2
ENST00000346085.10:c.3058_3059insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000344546.5:p.Thr1020ArgfsTer2
ENST00000350026.10:c.2770_2771insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000055163.7:p.Thr924ArgfsTer2
ENST00000414678.7:c.1177_1178insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000412835.2:p.Thr393ArgfsTer2
ENST00000452544.2:n.920_921insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC
ENST00000635849.1:c.340_341insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000490948.1:p.Thr114ArgfsTer2
ENST00000636426.1:n.153_154insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC
ENST00000636930.2:c.3019_3020insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC MANE Select	ENSP00000490491.2:p.Thr1007ArgfsTer2
ENST00000637015.1:c.258_259insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC
ENST00000637568.1:c.62_63insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC
ENST00000637810.1:c.520_521insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000489636.1:p.Thr174ArgfsTer2
ENST00000637904.1:c.520_521insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000490550.1:p.Thr174ArgfsTer2
ENST00000647938.1:c.2809_2810insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000498155.1:p.Thr937ArgfsTer2
ENST00000674190.1:n.1768_1769insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC
ENST00000319584.10:c.1036_1037insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000313006.6:p.Thr346ArgfsTer2
ENST00000346085.9:c.2809_2810insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000344546.4:p.Thr937ArgfsTer2
ENST00000350026.9:c.2770_2771insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000055163.7:p.Thr924ArgfsTer2
ENST00000414678.6:c.1177_1178insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	ENSP00000412835.2:p.Thr393ArgfsTer2
ENST00000452544.1:n.866_867insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC
ENST00000478761.3:c.92_93insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC
NM_017519.2:c.2770_2771insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	NP_059989.2:p.Thr924ArgfsTer2
NM_020732.3:c.2809_2810insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	NP_065783.3:p.Thr937ArgfsTer2
XM_005267069.3:c.2770_2771insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_005267126.2:p.Thr924ArgfsTer2
XM_011535984.1:c.1720_1721insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_011534286.1:p.Thr574ArgfsTer2
XM_011535985.1:c.1540_1541insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_011534287.1:p.Thr514ArgfsTer2
XM_011535986.1:c.1300_1301insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_011534288.1:p.Thr434ArgfsTer2
XM_011535987.1:c.919_920insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_011534289.1:p.Thr307ArgfsTer2
XM_011535988.1:c.-20+15674_-20+15675insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_011534290.1:n.-20+15674_-20+15675insGGTAACTACTCCAGACCCCCAG...
NM_001346813.1:c.2770_2771insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	NP_001333742.1:p.Thr924ArgfsTer2
NM_001363725.1:c.520_521insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	NP_001350654.1:p.Thr174ArgfsTer2
XM_011535984.2:c.2851_2852insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_011534286.2:p.Thr951ArgfsTer2
XM_011535988.3:c.-20+15674_-20+15675insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_011534290.1:n.-20+15674_-20+15675insGGTAACTACTCCAGACCCCCAG...
XM_017011103.2:c.2851_2852insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_016866592.1:p.Thr951ArgfsTer2
XM_017011104.1:c.2851_2852insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_016866593.1:p.Thr951ArgfsTer2
XM_017011105.2:c.2851_2852insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_016866594.1:p.Thr951ArgfsTer2
XM_017011106.2:c.2851_2852insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_016866595.1:p.Thr951ArgfsTer2
XM_017011107.2:c.2671_2672insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	XP_016866596.1:p.Thr891ArgfsTer2
XR_002956289.1:n.2934_2935insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC
NM_001363725.2:c.520_521insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	NP_001350654.1:p.Thr174ArgfsTer2
NM_001371656.1:c.3058_3059insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	NP_001358585.1:p.Thr1020ArgfsTer2
NM_001374820.1:c.3058_3059insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	NP_001361749.1:p.Thr1020ArgfsTer2
NM_001374828.1:c.3019_3020insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC MANE Select	NP_001361757.1:p.Thr1007ArgfsTer2
NM_017519.3:c.3019_3020insGGTAACTACTCCAGACCCCCAGCGTATAGTGGGGTGCC	NP_059989.3:p.Thr1007ArgfsTer2