Canonical Allele Identifier: CA645564752
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157206688del , CM000668.2:g.157206688del GRCh38
NC_000006.11:g.157527822del , CM000668.1:g.157527822del GRCh37
NC_000006.10:g.157569514del NCBI36
NG_032093.1:g.433759del
NG_032093.2:g.433759del
NG_066624.1:g.435663del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.5757del ENSP00000055163.8:p.Leu1920Ter
ENST00000414678.8:c.5826del ENSP00000412835.3:p.Leu1943Ter
ENST00000637015.2:c.6045del ENSP00000489729.2:p.Leu2016Ter
ENST00000346085.10:c.5796del ENSP00000344546.5:p.Leu1933Ter
ENST00000350026.10:c.5508del ENSP00000055163.7:p.Leu1837Ter
ENST00000414678.7:c.4074del ENSP00000412835.2:p.Leu1359Ter
ENST00000635849.1:c.3237del ENSP00000490948.1:p.Leu1080Ter
ENST00000635928.1:c.72del ENSP00000489717.1:p.Leu25Ter
ENST00000635957.1:c.2868del ENSP00000490385.1:p.Leu957Ter
ENST00000636227.1:n.4379del
ENST00000636254.1:n.1836del
ENST00000636930.2:c.5916del MANE Select ENSP00000490491.2:p.Leu1973Ter
ENST00000636940.1:n.3913del
ENST00000637015.1:c.3284del
ENST00000637568.1:c.3198del
ENST00000637741.1:n.2582del
ENST00000637810.1:c.3258del ENSP00000489636.1:p.Leu1087Ter
ENST00000637904.1:c.3417del ENSP00000490550.1:p.Leu1140Ter
ENST00000637933.1:n.3031del
ENST00000647938.1:c.5547del ENSP00000498155.1:p.Leu1850Ter
ENST00000346085.9:c.5547del ENSP00000344546.4:p.Leu1850Ter
ENST00000350026.9:c.5508del ENSP00000055163.7:p.Leu1837Ter
ENST00000414678.6:c.4074del ENSP00000412835.2:p.Leu1359Ter
NM_017519.2:c.5508del NP_059989.2:p.Leu1837Ter
NM_020732.3:c.5547del NP_065783.3:p.Leu1850Ter
XM_005267069.3:c.5667del XP_005267126.2:p.Leu1890Ter
XM_011535984.1:c.4746del XP_011534286.1:p.Leu1583Ter
XM_011535985.1:c.4566del XP_011534287.1:p.Leu1523Ter
XM_011535986.1:c.4326del XP_011534288.1:p.Leu1443Ter
XM_011535987.1:c.3945del XP_011534289.1:p.Leu1316Ter
XM_011535988.1:c.2808del XP_011534290.1:p.Leu937Ter
NM_001346813.1:c.5667del NP_001333742.1:p.Leu1890Ter
NM_001363725.1:c.3417del NP_001350654.1:p.Leu1140Ter
XM_011535984.2:c.5877del XP_011534286.2:p.Leu1960Ter
XM_011535988.3:c.2808del XP_011534290.1:p.Leu937Ter
XM_017011103.2:c.5778del XP_016866592.1:p.Leu1927Ter
XM_017011104.1:c.5748del XP_016866593.1:p.Leu1917Ter
XM_017011105.2:c.5718del XP_016866594.1:p.Leu1907Ter
XM_017011106.2:c.5589del XP_016866595.1:p.Leu1864Ter
XM_017011107.2:c.5568del XP_016866596.1:p.Leu1857Ter
XR_002956289.1:n.5863del
NM_001363725.2:c.3417del NP_001350654.1:p.Leu1140Ter
NM_001371656.1:c.5796del NP_001358585.1:p.Leu1933Ter
NM_001374820.1:c.5796del NP_001361749.1:p.Leu1933Ter
NM_001374828.1:c.5916del MANE Select NP_001361757.1:p.Leu1973Ter
NM_017519.3:c.5757del NP_059989.3:p.Leu1920Ter