Canonical Allele Identifier: CA16043414
Gene: ARID1B HGNC NCBI

Linked Data

ClinVar Variation Id: 374133
ClinVar RCV Id: RCV000415239
dbSNP Id: rs1057518918

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157184330del , CM000668.2:g.157184330del GRCh38
NC_000006.11:g.157505464del , CM000668.1:g.157505464del GRCh37
NC_000006.10:g.157547156del NCBI36
NG_032093.1:g.411401del
NG_032093.2:g.411401del
NG_066624.1:g.413305del

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.3655del ENSP00000055163.8:p.Leu1219CysfsTer?
ENST00000414678.8:c.3724del ENSP00000412835.3:p.Leu1242CysfsTer?
ENST00000637015.2:c.3943del ENSP00000489729.2:p.Leu1315CysfsTer?
ENST00000319584.11:c.1828del ENSP00000313006.7:p.Leu610CysfsTer?
ENST00000346085.10:c.3694del ENSP00000344546.5:p.Leu1232CysfsTer?
ENST00000350026.10:c.3406del ENSP00000055163.7:p.Leu1136CysfsTer?
ENST00000414678.7:c.1972del ENSP00000412835.2:p.Leu658CysfsTer?
ENST00000635849.1:c.1135del ENSP00000490948.1:p.Leu379CysfsTer?
ENST00000635957.1:c.769del ENSP00000490385.1:p.Leu257CysfsTer?
ENST00000636930.2:c.3814del MANE Select ENSP00000490491.2:p.Leu1272CysfsTer?
ENST00000636940.1:n.1811del
ENST00000637015.1:c.1182del
ENST00000637568.1:c.1096del
ENST00000637741.1:n.480del
ENST00000637810.1:c.1156del ENSP00000489636.1:p.Leu386CysfsTer?
ENST00000637904.1:c.1315del ENSP00000490550.1:p.Leu439CysfsTer?
ENST00000647938.1:c.3445del ENSP00000498155.1:p.Leu1149CysfsTer?
ENST00000319584.10:c.1831del ENSP00000313006.6:p.Leu611CysfsTer?
ENST00000346085.9:c.3445del ENSP00000344546.4:p.Leu1149CysfsTer?
ENST00000350026.9:c.3406del ENSP00000055163.7:p.Leu1136CysfsTer?
ENST00000400790.3:c.607del ENSP00000383596.3:p.Leu203CysfsTer?
ENST00000414678.6:c.1972del ENSP00000412835.2:p.Leu658CysfsTer?
NM_017519.2:c.3406del NP_059989.2:p.Leu1136CysfsTer?
NM_020732.3:c.3445del NP_065783.3:p.Leu1149CysfsTer?
XM_005267069.3:c.3565del XP_005267126.2:p.Leu1189CysfsTer?
XM_011535984.1:c.2644del XP_011534286.1:p.Leu882CysfsTer?
XM_011535985.1:c.2464del XP_011534287.1:p.Leu822CysfsTer?
XM_011535986.1:c.2224del XP_011534288.1:p.Leu742CysfsTer?
XM_011535987.1:c.1843del XP_011534289.1:p.Leu615CysfsTer?
XM_011535988.1:c.706del XP_011534290.1:p.Leu236CysfsTer?
NM_001346813.1:c.3565del NP_001333742.1:p.Leu1189CysfsTer?
NM_001363725.1:c.1315del NP_001350654.1:p.Leu439CysfsTer?
XM_011535984.2:c.3775del XP_011534286.2:p.Leu1259CysfsTer?
XM_011535988.3:c.706del XP_011534290.1:p.Leu236CysfsTer?
XM_017011103.2:c.3676del XP_016866592.1:p.Leu1226CysfsTer?
XM_017011104.1:c.3646del XP_016866593.1:p.Leu1216CysfsTer?
XM_017011105.2:c.3616del XP_016866594.1:p.Leu1206CysfsTer?
XM_017011106.2:c.3487del XP_016866595.1:p.Leu1163CysfsTer?
XM_017011107.2:c.3466del XP_016866596.1:p.Leu1156CysfsTer?
XR_002956289.1:n.3858del
NM_001363725.2:c.1315del NP_001350654.1:p.Leu439CysfsTer?
NM_001371656.1:c.3694del NP_001358585.1:p.Leu1232CysfsTer?
NM_001374820.1:c.3694del NP_001361749.1:p.Leu1232CysfsTer?
NM_001374828.1:c.3814del MANE Select NP_001361757.1:p.Leu1272CysfsTer?
NM_017519.3:c.3655del NP_059989.3:p.Leu1219CysfsTer?