Canonical Allele Identifier: CA658796860

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 498830
• ClinVar RCV Id: RCV000596725 ; RCV002470920
• dbSNP Id: rs1554233122

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190126_157190128delinsAG , CM000668.2:g.157190126_157190128delinsAG	GRCh38
NC_000006.11:g.157511260_157511262delinsAG , CM000668.1:g.157511260_157511262delinsAG	GRCh37
NC_000006.10:g.157552952_157552954delinsAG	NCBI36
NG_032093.1:g.417197_417199delinsAG
NG_032093.2:g.417197_417199delinsAG
NG_066624.1:g.419101_419103delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3988_3990delinsAG	ENSP00000055163.8:p.Tyr1330SerfsTer5
ENST00000414678.8:c.4057_4059delinsAG	ENSP00000412835.3:p.Tyr1353SerfsTer5
ENST00000637015.2:c.4276_4278delinsAG	ENSP00000489729.2:p.Tyr1426SerfsTer5
ENST00000346085.10:c.4027_4029delinsAG	ENSP00000344546.5:p.Tyr1343SerfsTer5
ENST00000350026.10:c.3739_3741delinsAG	ENSP00000055163.7:p.Tyr1247SerfsTer5
ENST00000414678.7:c.2305_2307delinsAG	ENSP00000412835.2:p.Tyr769SerfsTer5
ENST00000635849.1:c.1468_1470delinsAG	ENSP00000490948.1:p.Tyr490SerfsTer5
ENST00000635957.1:c.1099_1101delinsAG	ENSP00000490385.1:p.Tyr367SerfsTer5
ENST00000636930.2:c.4147_4149delinsAG MANE Select	ENSP00000490491.2:p.Tyr1383SerfsTer5
ENST00000636940.1:n.2144_2146delinsAG
ENST00000637015.1:c.1515_1517delinsAG
ENST00000637568.1:c.1429_1431delinsAG
ENST00000637741.1:n.813_815delinsAG
ENST00000637810.1:c.1489_1491delinsAG	ENSP00000489636.1:p.Tyr497SerfsTer5
ENST00000637904.1:c.1648_1650delinsAG	ENSP00000490550.1:p.Tyr550SerfsTer5
ENST00000647938.1:c.3778_3780delinsAG	ENSP00000498155.1:p.Tyr1260SerfsTer5
ENST00000346085.9:c.3778_3780delinsAG	ENSP00000344546.4:p.Tyr1260SerfsTer5
ENST00000350026.9:c.3739_3741delinsAG	ENSP00000055163.7:p.Tyr1247SerfsTer5
ENST00000414678.6:c.2305_2307delinsAG	ENSP00000412835.2:p.Tyr769SerfsTer5
NM_017519.2:c.3739_3741delinsAG	NP_059989.2:p.Tyr1247SerfsTer5
NM_020732.3:c.3778_3780delinsAG	NP_065783.3:p.Tyr1260SerfsTer5
XM_005267069.3:c.3898_3900delinsAG	XP_005267126.2:p.Tyr1300SerfsTer5
XM_011535984.1:c.2977_2979delinsAG	XP_011534286.1:p.Tyr993SerfsTer5
XM_011535985.1:c.2797_2799delinsAG	XP_011534287.1:p.Tyr933SerfsTer5
XM_011535986.1:c.2557_2559delinsAG	XP_011534288.1:p.Tyr853SerfsTer5
XM_011535987.1:c.2176_2178delinsAG	XP_011534289.1:p.Tyr726SerfsTer5
XM_011535988.1:c.1039_1041delinsAG	XP_011534290.1:p.Tyr347SerfsTer5
NM_001346813.1:c.3898_3900delinsAG	NP_001333742.1:p.Tyr1300SerfsTer5
NM_001363725.1:c.1648_1650delinsAG	NP_001350654.1:p.Tyr550SerfsTer5
XM_011535984.2:c.4108_4110delinsAG	XP_011534286.2:p.Tyr1370SerfsTer5
XM_011535988.3:c.1039_1041delinsAG	XP_011534290.1:p.Tyr347SerfsTer5
XM_017011103.2:c.4009_4011delinsAG	XP_016866592.1:p.Tyr1337SerfsTer5
XM_017011104.1:c.3979_3981delinsAG	XP_016866593.1:p.Tyr1327SerfsTer5
XM_017011105.2:c.3949_3951delinsAG	XP_016866594.1:p.Tyr1317SerfsTer5
XM_017011106.2:c.3820_3822delinsAG	XP_016866595.1:p.Tyr1274SerfsTer5
XM_017011107.2:c.3799_3801delinsAG	XP_016866596.1:p.Tyr1267SerfsTer5
XR_002956289.1:n.4191_4193delinsAG
NM_001363725.2:c.1648_1650delinsAG	NP_001350654.1:p.Tyr550SerfsTer5
NM_001371656.1:c.4027_4029delinsAG	NP_001358585.1:p.Tyr1343SerfsTer5
NM_001374820.1:c.4027_4029delinsAG	NP_001361749.1:p.Tyr1343SerfsTer5
NM_001374828.1:c.4147_4149delinsAG MANE Select	NP_001361757.1:p.Tyr1383SerfsTer5
NM_017519.3:c.3988_3990delinsAG	NP_059989.3:p.Tyr1330SerfsTer5