Canonical Allele Identifier: CA1675343584
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156778557_156778599delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC , CM000668.2:g.156778557_156778599delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC GRCh38
NC_000006.11:g.157099691_157099733delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC , CM000668.1:g.157099691_157099733delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC GRCh37
NC_000006.10:g.157141383_157141425delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC NCBI36
NG_032093.1:g.5628_5670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC
NG_032093.2:g.5628_5670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC
NG_066624.1:g.7532_7574delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.877_919delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC ENSP00000055163.8:p.Thr293=
ENST00000414678.8:c.877_919delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC ENSP00000412835.3:p.Thr293=
ENST00000637015.2:c.877_919delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC ENSP00000489729.2:p.Thr293=
ENST00000346085.10:c.877_919delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC ENSP00000344546.5:p.Thr293=
ENST00000350026.10:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC ENSP00000055163.7:p.Thr210=
ENST00000636930.2:c.877_919delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC MANE Select ENSP00000490491.2:p.Thr293=
ENST00000647938.1:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC ENSP00000498155.1:p.Thr210=
ENST00000674298.1:c.617_659delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC
ENST00000346085.9:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC ENSP00000344546.4:p.Thr210=
ENST00000350026.9:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC ENSP00000055163.7:p.Thr210=
NM_017519.2:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC NP_059989.2:p.Thr210=
NM_020732.3:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC NP_065783.3:p.Thr210=
XM_005267069.3:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC XP_005267126.2:p.Thr210=
NM_001346813.1:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC NP_001333742.1:p.Thr210=
XM_011535984.2:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC XP_011534286.2:p.Thr210=
XM_017011103.2:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC XP_016866592.1:p.Thr210=
XM_017011104.1:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC XP_016866593.1:p.Thr210=
XM_017011105.2:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC XP_016866594.1:p.Thr210=
XM_017011106.2:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC XP_016866595.1:p.Thr210=
XM_017011107.2:c.628_670delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC XP_016866596.1:p.Thr210=
XR_002956289.1:n.711_753delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC
NM_001371656.1:c.877_919delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC NP_001358585.1:p.Thr293=
NM_001374820.1:c.877_919delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC NP_001361749.1:p.Thr293=
NM_001374828.1:c.877_919delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC MANE Select NP_001361757.1:p.Thr293=
NM_017519.3:c.877_919delinsACGCAGCAGCCGCCGGTCGCCGTGCCCGGGGGCGGCGGCGGCC NP_059989.3:p.Thr293=