Canonical Allele Identifier: CA2580075259
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157174033del , CM000668.2:g.157174033del GRCh38
NC_000006.11:g.157495167del , CM000668.1:g.157495167del GRCh37
NC_000006.10:g.157536859del NCBI36
NG_032093.1:g.401104del
NG_032093.2:g.401104del
NG_066624.1:g.403008del

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.3261del MANE Select NP_001361757.1:p.Met1087IlefsTer?
ENST00000636930.2:c.3261del MANE Select ENSP00000490491.2:p.Met1087IlefsTer?
NM_001346813.1:c.3012del NP_001333742.1:p.Met1004IlefsTer?
NM_001363725.1:c.762del NP_001350654.1:p.Met254IlefsTer?
NM_001363725.2:c.762del NP_001350654.1:p.Met254IlefsTer?
NM_001371656.1:c.3300del NP_001358585.1:p.Met1100IlefsTer?
NM_001374820.1:c.3300del NP_001361749.1:p.Met1100IlefsTer?
NM_017519.2:c.3012del NP_059989.2:p.Met1004IlefsTer?
NM_017519.3:c.3261del NP_059989.3:p.Met1087IlefsTer?
NM_020732.3:c.3051del NP_065783.3:p.Met1017IlefsTer?
ENST00000319584.10:c.1278del ENSP00000313006.6:p.Met426IlefsTer?
ENST00000319584.11:c.1275del ENSP00000313006.7:p.Met425IlefsTer?
ENST00000346085.10:c.3300del ENSP00000344546.5:p.Met1100IlefsTer?
ENST00000346085.9:c.3051del ENSP00000344546.4:p.Met1017IlefsTer?
ENST00000350026.10:c.3012del ENSP00000055163.7:p.Met1004IlefsTer?
ENST00000350026.11:c.3261del ENSP00000055163.8:p.Met1087IlefsTer?
ENST00000350026.9:c.3012del ENSP00000055163.7:p.Met1004IlefsTer?
ENST00000400790.3:c.213del ENSP00000383596.3:p.Met71IlefsTer?
ENST00000414678.6:c.1419del ENSP00000412835.2:p.Met473IlefsTer?
ENST00000414678.7:c.1419del ENSP00000412835.2:p.Met473IlefsTer?
ENST00000414678.8:c.3171del ENSP00000412835.3:p.Met1057IlefsTer?
ENST00000478761.3:c.463del
ENST00000478761.4:n.49del
ENST00000635849.1:c.582del ENSP00000490948.1:p.Met194IlefsTer?
ENST00000635957.1:c.216del ENSP00000490385.1:p.Met72IlefsTer?
ENST00000636940.1:n.1258del
ENST00000637015.1:c.629del
ENST00000637015.2:c.3390del ENSP00000489729.2:p.Met1130IlefsTer?
ENST00000637170.1:n.533del
ENST00000637568.1:c.543del
ENST00000637741.1:n.86del
ENST00000637810.1:c.762del ENSP00000489636.1:p.Met254IlefsTer?
ENST00000637904.1:c.762del ENSP00000490550.1:p.Met254IlefsTer?
ENST00000647938.1:c.3051del ENSP00000498155.1:p.Met1017IlefsTer?
XM_005267069.3:c.3012del XP_005267126.2:p.Met1004IlefsTer?
XM_011535984.1:c.2091del XP_011534286.1:p.Met697IlefsTer?
XM_011535984.2:c.3222del XP_011534286.2:p.Met1074IlefsTer?
XM_011535985.1:c.1911del XP_011534287.1:p.Met637IlefsTer?
XM_011535986.1:c.1671del XP_011534288.1:p.Met557IlefsTer?
XM_011535987.1:c.1290del XP_011534289.1:p.Met430IlefsTer?
XM_011535988.1:c.153del XP_011534290.1:p.Met51IlefsTer?
XM_011535988.3:c.153del XP_011534290.1:p.Met51IlefsTer?
XM_017011103.2:c.3123del XP_016866592.1:p.Met1041IlefsTer?
XM_017011104.1:c.3093del XP_016866593.1:p.Met1031IlefsTer?
XM_017011105.2:c.3222del XP_016866594.1:p.Met1074IlefsTer?
XM_017011106.2:c.3093del XP_016866595.1:p.Met1031IlefsTer?
XM_017011107.2:c.2913del XP_016866596.1:p.Met971IlefsTer?
XR_002956289.1:n.3305del