Canonical Allele Identifier: CA923726193

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190126del , CM000668.2:g.157190126del	GRCh38
NC_000006.11:g.157511260del , CM000668.1:g.157511260del	GRCh37
NC_000006.10:g.157552952del	NCBI36
NG_032093.1:g.417197del
NG_032093.2:g.417197del
NG_066624.1:g.419101del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3988del	ENSP00000055163.8:p.Tyr1330ThrfsTer5
ENST00000414678.8:c.4057del	ENSP00000412835.3:p.Tyr1353ThrfsTer5
ENST00000637015.2:c.4276del	ENSP00000489729.2:p.Tyr1426ThrfsTer5
ENST00000346085.10:c.4027del	ENSP00000344546.5:p.Tyr1343ThrfsTer5
ENST00000350026.10:c.3739del	ENSP00000055163.7:p.Tyr1247ThrfsTer5
ENST00000414678.7:c.2305del	ENSP00000412835.2:p.Tyr769ThrfsTer5
ENST00000635849.1:c.1468del	ENSP00000490948.1:p.Tyr490ThrfsTer5
ENST00000635957.1:c.1099del	ENSP00000490385.1:p.Tyr367ThrfsTer5
ENST00000636930.2:c.4147del MANE Select	ENSP00000490491.2:p.Tyr1383ThrfsTer5
ENST00000636940.1:n.2144del
ENST00000637015.1:c.1515del
ENST00000637568.1:c.1429del
ENST00000637741.1:n.813del
ENST00000637810.1:c.1489del	ENSP00000489636.1:p.Tyr497ThrfsTer5
ENST00000637904.1:c.1648del	ENSP00000490550.1:p.Tyr550ThrfsTer5
ENST00000647938.1:c.3778del	ENSP00000498155.1:p.Tyr1260ThrfsTer5
ENST00000346085.9:c.3778del	ENSP00000344546.4:p.Tyr1260ThrfsTer5
ENST00000350026.9:c.3739del	ENSP00000055163.7:p.Tyr1247ThrfsTer5
ENST00000414678.6:c.2305del	ENSP00000412835.2:p.Tyr769ThrfsTer5
NM_017519.2:c.3739del	NP_059989.2:p.Tyr1247ThrfsTer5
NM_020732.3:c.3778del	NP_065783.3:p.Tyr1260ThrfsTer5
XM_005267069.3:c.3898del	XP_005267126.2:p.Tyr1300ThrfsTer5
XM_011535984.1:c.2977del	XP_011534286.1:p.Tyr993ThrfsTer5
XM_011535985.1:c.2797del	XP_011534287.1:p.Tyr933ThrfsTer5
XM_011535986.1:c.2557del	XP_011534288.1:p.Tyr853ThrfsTer5
XM_011535987.1:c.2176del	XP_011534289.1:p.Tyr726ThrfsTer5
XM_011535988.1:c.1039del	XP_011534290.1:p.Tyr347ThrfsTer5
NM_001346813.1:c.3898del	NP_001333742.1:p.Tyr1300ThrfsTer5
NM_001363725.1:c.1648del	NP_001350654.1:p.Tyr550ThrfsTer5
XM_011535984.2:c.4108del	XP_011534286.2:p.Tyr1370ThrfsTer5
XM_011535988.3:c.1039del	XP_011534290.1:p.Tyr347ThrfsTer5
XM_017011103.2:c.4009del	XP_016866592.1:p.Tyr1337ThrfsTer5
XM_017011104.1:c.3979del	XP_016866593.1:p.Tyr1327ThrfsTer5
XM_017011105.2:c.3949del	XP_016866594.1:p.Tyr1317ThrfsTer5
XM_017011106.2:c.3820del	XP_016866595.1:p.Tyr1274ThrfsTer5
XM_017011107.2:c.3799del	XP_016866596.1:p.Tyr1267ThrfsTer5
XR_002956289.1:n.4191del
NM_001363725.2:c.1648del	NP_001350654.1:p.Tyr550ThrfsTer5
NM_001371656.1:c.4027del	NP_001358585.1:p.Tyr1343ThrfsTer5
NM_001374820.1:c.4027del	NP_001361749.1:p.Tyr1343ThrfsTer5
NM_001374828.1:c.4147del MANE Select	NP_001361757.1:p.Tyr1383ThrfsTer5
NM_017519.3:c.3988del	NP_059989.3:p.Tyr1330ThrfsTer5