Canonical Allele Identifier: CA2580075265

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2444091
• ClinVar RCV Id: RCV003152889

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189655del , CM000668.2:g.157189655del	GRCh38
NC_000006.11:g.157510789del , CM000668.1:g.157510789del	GRCh37
NC_000006.10:g.157552481del	NCBI36
NG_032093.1:g.416726del
NG_032093.2:g.416726del
NG_066624.1:g.418630del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3774del	ENSP00000055163.8:p.Leu1259CysfsTer22
ENST00000414678.8:c.3843del	ENSP00000412835.3:p.Leu1282CysfsTer22
ENST00000637015.2:c.4062del	ENSP00000489729.2:p.Leu1355CysfsTer22
ENST00000346085.10:c.3813del	ENSP00000344546.5:p.Leu1272CysfsTer22
ENST00000350026.10:c.3525del	ENSP00000055163.7:p.Leu1176CysfsTer22
ENST00000414678.7:c.2091del	ENSP00000412835.2:p.Leu698CysfsTer22
ENST00000635849.1:c.1254del	ENSP00000490948.1:p.Leu419CysfsTer22
ENST00000635957.1:c.888del	ENSP00000490385.1:p.Leu297CysfsTer22
ENST00000636930.2:c.3933del MANE Select	ENSP00000490491.2:p.Leu1312CysfsTer22
ENST00000636940.1:n.1930del
ENST00000637015.1:c.1301del
ENST00000637568.1:c.1215del
ENST00000637741.1:n.599del
ENST00000637810.1:c.1275del	ENSP00000489636.1:p.Leu426CysfsTer22
ENST00000637904.1:c.1434del	ENSP00000490550.1:p.Leu479CysfsTer22
ENST00000647938.1:c.3564del	ENSP00000498155.1:p.Leu1189CysfsTer22
ENST00000346085.9:c.3564del	ENSP00000344546.4:p.Leu1189CysfsTer22
ENST00000350026.9:c.3525del	ENSP00000055163.7:p.Leu1176CysfsTer22
ENST00000414678.6:c.2091del	ENSP00000412835.2:p.Leu698CysfsTer22
NM_017519.2:c.3525del	NP_059989.2:p.Leu1176CysfsTer22
NM_020732.3:c.3564del	NP_065783.3:p.Leu1189CysfsTer22
XM_005267069.3:c.3684del	XP_005267126.2:p.Leu1229CysfsTer22
XM_011535984.1:c.2763del	XP_011534286.1:p.Leu922CysfsTer22
XM_011535985.1:c.2583del	XP_011534287.1:p.Leu862CysfsTer22
XM_011535986.1:c.2343del	XP_011534288.1:p.Leu782CysfsTer22
XM_011535987.1:c.1962del	XP_011534289.1:p.Leu655CysfsTer22
XM_011535988.1:c.825del	XP_011534290.1:p.Leu276CysfsTer22
NM_001346813.1:c.3684del	NP_001333742.1:p.Leu1229CysfsTer22
NM_001363725.1:c.1434del	NP_001350654.1:p.Leu479CysfsTer22
XM_011535984.2:c.3894del	XP_011534286.2:p.Leu1299CysfsTer22
XM_011535988.3:c.825del	XP_011534290.1:p.Leu276CysfsTer22
XM_017011103.2:c.3795del	XP_016866592.1:p.Leu1266CysfsTer22
XM_017011104.1:c.3765del	XP_016866593.1:p.Leu1256CysfsTer22
XM_017011105.2:c.3735del	XP_016866594.1:p.Leu1246CysfsTer22
XM_017011106.2:c.3606del	XP_016866595.1:p.Leu1203CysfsTer22
XM_017011107.2:c.3585del	XP_016866596.1:p.Leu1196CysfsTer22
XR_002956289.1:n.3977del
NM_001363725.2:c.1434del	NP_001350654.1:p.Leu479CysfsTer22
NM_001371656.1:c.3813del	NP_001358585.1:p.Leu1272CysfsTer22
NM_001374820.1:c.3813del	NP_001361749.1:p.Leu1272CysfsTer22
NM_001374828.1:c.3933del MANE Select	NP_001361757.1:p.Leu1312CysfsTer22
NM_017519.3:c.3774del	NP_059989.3:p.Leu1259CysfsTer22