Canonical Allele Identifier: CA2573102951

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1805388
• ClinVar RCV Id: RCV002471806

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157180996del , CM000668.2:g.157180996del	GRCh38
NC_000006.11:g.157502130del , CM000668.1:g.157502130del	GRCh37
NC_000006.10:g.157543822del	NCBI36
NG_032093.1:g.408067del
NG_032093.2:g.408067del
NG_066624.1:g.409971del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3373del	ENSP00000055163.8:p.Glu1125ArgfsTer?
ENST00000414678.8:c.3442del	ENSP00000412835.3:p.Glu1148ArgfsTer?
ENST00000637015.2:c.3661del	ENSP00000489729.2:p.Glu1221ArgfsTer?
ENST00000319584.11:c.1546del	ENSP00000313006.7:p.Glu516ArgfsTer?
ENST00000346085.10:c.3412del	ENSP00000344546.5:p.Glu1138ArgfsTer?
ENST00000350026.10:c.3124del	ENSP00000055163.7:p.Glu1042ArgfsTer?
ENST00000414678.7:c.1690del	ENSP00000412835.2:p.Glu564ArgfsTer?
ENST00000635849.1:c.853del	ENSP00000490948.1:p.Glu285ArgfsTer?
ENST00000635957.1:c.487del	ENSP00000490385.1:p.Glu163ArgfsTer?
ENST00000636930.2:c.3532del MANE Select	ENSP00000490491.2:p.Glu1178ArgfsTer?
ENST00000636940.1:n.1529del
ENST00000637015.1:c.900del
ENST00000637568.1:c.814del
ENST00000637741.1:n.198del
ENST00000637810.1:c.874del	ENSP00000489636.1:p.Glu292ArgfsTer?
ENST00000637904.1:c.1033del	ENSP00000490550.1:p.Glu345ArgfsTer?
ENST00000647938.1:c.3163del	ENSP00000498155.1:p.Glu1055ArgfsTer?
ENST00000319584.10:c.1549del	ENSP00000313006.6:p.Glu517ArgfsTer?
ENST00000346085.9:c.3163del	ENSP00000344546.4:p.Glu1055ArgfsTer?
ENST00000350026.9:c.3124del	ENSP00000055163.7:p.Glu1042ArgfsTer?
ENST00000400790.3:c.325del	ENSP00000383596.3:p.Glu109ArgfsTer?
ENST00000414678.6:c.1690del	ENSP00000412835.2:p.Glu564ArgfsTer?
ENST00000478761.3:c.734del
NM_017519.2:c.3124del	NP_059989.2:p.Glu1042ArgfsTer?
NM_020732.3:c.3163del	NP_065783.3:p.Glu1055ArgfsTer?
XM_005267069.3:c.3283del	XP_005267126.2:p.Glu1095ArgfsTer?
XM_011535984.1:c.2362del	XP_011534286.1:p.Glu788ArgfsTer?
XM_011535985.1:c.2182del	XP_011534287.1:p.Glu728ArgfsTer?
XM_011535986.1:c.1942del	XP_011534288.1:p.Glu648ArgfsTer?
XM_011535987.1:c.1561del	XP_011534289.1:p.Glu521ArgfsTer?
XM_011535988.1:c.424del	XP_011534290.1:p.Glu142ArgfsTer?
NM_001346813.1:c.3283del	NP_001333742.1:p.Glu1095ArgfsTer?
NM_001363725.1:c.1033del	NP_001350654.1:p.Glu345ArgfsTer?
XM_011535984.2:c.3493del	XP_011534286.2:p.Glu1165ArgfsTer?
XM_011535988.3:c.424del	XP_011534290.1:p.Glu142ArgfsTer?
XM_017011103.2:c.3394del	XP_016866592.1:p.Glu1132ArgfsTer?
XM_017011104.1:c.3364del	XP_016866593.1:p.Glu1122ArgfsTer?
XM_017011105.2:c.3334del	XP_016866594.1:p.Glu1112ArgfsTer?
XM_017011106.2:c.3205del	XP_016866595.1:p.Glu1069ArgfsTer?
XM_017011107.2:c.3184del	XP_016866596.1:p.Glu1062ArgfsTer?
XR_002956289.1:n.3576del
NM_001363725.2:c.1033del	NP_001350654.1:p.Glu345ArgfsTer?
NM_001371656.1:c.3412del	NP_001358585.1:p.Glu1138ArgfsTer?
NM_001374820.1:c.3412del	NP_001361749.1:p.Glu1138ArgfsTer?
NM_001374828.1:c.3532del MANE Select	NP_001361757.1:p.Glu1178ArgfsTer?
NM_017519.3:c.3373del	NP_059989.3:p.Glu1125ArgfsTer?