Canonical Allele Identifier: CA658655964
Gene: ARID1B HGNC NCBI

Linked Data

ClinVar Variation Id: 451580
ClinVar RCV Id: RCV000519776
dbSNP Id: rs1554231830

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157184313del , CM000668.2:g.157184313del GRCh38
NC_000006.11:g.157505447del , CM000668.1:g.157505447del GRCh37
NC_000006.10:g.157547139del NCBI36
NG_032093.1:g.411384del
NG_032093.2:g.411384del
NG_066624.1:g.413288del

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.3638del ENSP00000055163.8:p.Lys1213SerfsTer?
ENST00000414678.8:c.3707del ENSP00000412835.3:p.Lys1236SerfsTer?
ENST00000637015.2:c.3926del ENSP00000489729.2:p.Lys1309SerfsTer?
ENST00000319584.11:c.1811del ENSP00000313006.7:p.Lys604SerfsTer?
ENST00000346085.10:c.3677del ENSP00000344546.5:p.Lys1226SerfsTer?
ENST00000350026.10:c.3389del ENSP00000055163.7:p.Lys1130SerfsTer?
ENST00000414678.7:c.1955del ENSP00000412835.2:p.Lys652SerfsTer?
ENST00000635849.1:c.1118del ENSP00000490948.1:p.Lys373SerfsTer?
ENST00000635957.1:c.752del ENSP00000490385.1:p.Lys251SerfsTer?
ENST00000636930.2:c.3797del MANE Select ENSP00000490491.2:p.Lys1266SerfsTer?
ENST00000636940.1:n.1794del
ENST00000637015.1:c.1165del
ENST00000637568.1:c.1079del
ENST00000637741.1:n.463del
ENST00000637810.1:c.1139del ENSP00000489636.1:p.Lys380SerfsTer?
ENST00000637904.1:c.1298del ENSP00000490550.1:p.Lys433SerfsTer?
ENST00000647938.1:c.3428del ENSP00000498155.1:p.Lys1143SerfsTer?
ENST00000319584.10:c.1814del ENSP00000313006.6:p.Lys605SerfsTer?
ENST00000346085.9:c.3428del ENSP00000344546.4:p.Lys1143SerfsTer?
ENST00000350026.9:c.3389del ENSP00000055163.7:p.Lys1130SerfsTer?
ENST00000400790.3:c.590del ENSP00000383596.3:p.Lys197SerfsTer?
ENST00000414678.6:c.1955del ENSP00000412835.2:p.Lys652SerfsTer?
NM_017519.2:c.3389del NP_059989.2:p.Lys1130SerfsTer?
NM_020732.3:c.3428del NP_065783.3:p.Lys1143SerfsTer?
XM_005267069.3:c.3548del XP_005267126.2:p.Lys1183SerfsTer?
XM_011535984.1:c.2627del XP_011534286.1:p.Lys876SerfsTer?
XM_011535985.1:c.2447del XP_011534287.1:p.Lys816SerfsTer?
XM_011535986.1:c.2207del XP_011534288.1:p.Lys736SerfsTer?
XM_011535987.1:c.1826del XP_011534289.1:p.Lys609SerfsTer?
XM_011535988.1:c.689del XP_011534290.1:p.Lys230SerfsTer?
NM_001346813.1:c.3548del NP_001333742.1:p.Lys1183SerfsTer?
NM_001363725.1:c.1298del NP_001350654.1:p.Lys433SerfsTer?
XM_011535984.2:c.3758del XP_011534286.2:p.Lys1253SerfsTer?
XM_011535988.3:c.689del XP_011534290.1:p.Lys230SerfsTer?
XM_017011103.2:c.3659del XP_016866592.1:p.Lys1220SerfsTer?
XM_017011104.1:c.3629del XP_016866593.1:p.Lys1210SerfsTer?
XM_017011105.2:c.3599del XP_016866594.1:p.Lys1200SerfsTer?
XM_017011106.2:c.3470del XP_016866595.1:p.Lys1157SerfsTer?
XM_017011107.2:c.3449del XP_016866596.1:p.Lys1150SerfsTer?
XR_002956289.1:n.3841del
NM_001363725.2:c.1298del NP_001350654.1:p.Lys433SerfsTer?
NM_001371656.1:c.3677del NP_001358585.1:p.Lys1226SerfsTer?
NM_001374820.1:c.3677del NP_001361749.1:p.Lys1226SerfsTer?
NM_001374828.1:c.3797del MANE Select NP_001361757.1:p.Lys1266SerfsTer?
NM_017519.3:c.3638del NP_059989.3:p.Lys1213SerfsTer?