Canonical Allele Identifier: CA2961565382
Community Standard Title: NM_001374828.1(ARID1B):c.3037_3038del (p.Gln1013GlyfsTer?)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157148899_157148900del , CM000668.2:g.157148899_157148900del GRCh38
NC_000006.11:g.157470033_157470034del , CM000668.1:g.157470033_157470034del GRCh37
NC_000006.10:g.157511725_157511726del NCBI36
NG_032093.1:g.375970_375971del
NG_032093.2:g.375970_375971del
NG_066624.1:g.377874_377875del

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.3037_3038del MANE Select NP_001361757.1:p.Gln1013GlyfsTer?
ENST00000636930.2:c.3037_3038del MANE Select ENSP00000490491.2:p.Gln1013GlyfsTer?
NM_001346813.1:c.2788_2789del NP_001333742.1:p.Gln930GlyfsTer?
NM_001363725.1:c.538_539del NP_001350654.1:p.Gln180GlyfsTer?
NM_001363725.2:c.538_539del NP_001350654.1:p.Gln180GlyfsTer?
NM_001371656.1:c.3076_3077del NP_001358585.1:p.Gln1026GlyfsTer?
NM_001374820.1:c.3076_3077del NP_001361749.1:p.Gln1026GlyfsTer?
NM_017519.2:c.2788_2789del NP_059989.2:p.Gln930GlyfsTer?
NM_017519.3:c.3037_3038del NP_059989.3:p.Gln1013GlyfsTer?
NM_020732.3:c.2827_2828del NP_065783.3:p.Gln943GlyfsTer?
ENST00000319584.10:c.1054_1055del ENSP00000313006.6:p.Gln352GlyfsTer?
ENST00000319584.11:c.1051_1052del ENSP00000313006.7:p.Gln351GlyfsTer?
ENST00000346085.10:c.3076_3077del ENSP00000344546.5:p.Gln1026GlyfsTer?
ENST00000346085.9:c.2827_2828del ENSP00000344546.4:p.Gln943GlyfsTer?
ENST00000350026.10:c.2788_2789del ENSP00000055163.7:p.Gln930GlyfsTer?
ENST00000350026.11:c.3037_3038del ENSP00000055163.8:p.Gln1013GlyfsTer?
ENST00000350026.9:c.2788_2789del ENSP00000055163.7:p.Gln930GlyfsTer?
ENST00000414678.6:c.1195_1196del ENSP00000412835.2:p.Gln399GlyfsTer?
ENST00000414678.7:c.1195_1196del ENSP00000412835.2:p.Gln399GlyfsTer?
ENST00000414678.8:c.2947_2948del ENSP00000412835.3:p.Gln983GlyfsTer?
ENST00000452544.1:n.884_885del
ENST00000452544.2:n.938_939del
ENST00000478761.3:c.110_111del
ENST00000635849.1:c.358_359del ENSP00000490948.1:p.Gln120GlyfsTer?
ENST00000636426.1:n.171_172del
ENST00000637015.1:c.276_277del
ENST00000637015.2:c.3037_3038del ENSP00000489729.2:p.Gln1013GlyfsTer22
ENST00000637568.1:c.80_81del
ENST00000637810.1:c.538_539del ENSP00000489636.1:p.Gln180GlyfsTer?
ENST00000637904.1:c.538_539del ENSP00000490550.1:p.Gln180GlyfsTer?
ENST00000647938.1:c.2827_2828del ENSP00000498155.1:p.Gln943GlyfsTer?
ENST00000674190.1:n.1786_1787del
XM_005267069.3:c.2788_2789del XP_005267126.2:p.Gln930GlyfsTer?
XM_011535984.1:c.1738_1739del XP_011534286.1:p.Gln580GlyfsTer22
XM_011535984.2:c.2869_2870del XP_011534286.2:p.Gln957GlyfsTer22
XM_011535985.1:c.1558_1559del XP_011534287.1:p.Gln520GlyfsTer22
XM_011535986.1:c.1318_1319del XP_011534288.1:p.Gln440GlyfsTer22
XM_011535987.1:c.937_938del XP_011534289.1:p.Gln313GlyfsTer22
XM_011535988.1:c.-20+15692_-20+15693del XP_011534290.1:n.-20+15692_-20+15693del
XM_011535988.3:c.-20+15692_-20+15693del XP_011534290.1:n.-20+15692_-20+15693del
XM_017011103.2:c.2869_2870del XP_016866592.1:p.Gln957GlyfsTer?
XM_017011104.1:c.2869_2870del XP_016866593.1:p.Gln957GlyfsTer?
XM_017011105.2:c.2869_2870del XP_016866594.1:p.Gln957GlyfsTer22
XM_017011106.2:c.2869_2870del XP_016866595.1:p.Gln957GlyfsTer?
XM_017011107.2:c.2689_2690del XP_016866596.1:p.Gln897GlyfsTer?
XR_002956289.1:n.2952_2953del