Canonical Allele Identifier: CA2739289477

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201072del , CM000668.2:g.157201072del	GRCh38
NC_000006.11:g.157522206del , CM000668.1:g.157522206del	GRCh37
NC_000006.10:g.157563898del	NCBI36
NG_032093.1:g.428143del
NG_032093.2:g.428143del
NG_066624.1:g.430047del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4688del	ENSP00000055163.8:p.Met1563ArgfsTer7
ENST00000414678.8:c.4757del	ENSP00000412835.3:p.Met1586ArgfsTer7
ENST00000637015.2:c.4976del	ENSP00000489729.2:p.Met1659ArgfsTer7
ENST00000346085.10:c.4727del	ENSP00000344546.5:p.Met1576ArgfsTer7
ENST00000350026.10:c.4439del	ENSP00000055163.7:p.Met1480ArgfsTer7
ENST00000414678.7:c.3005del	ENSP00000412835.2:p.Met1002ArgfsTer7
ENST00000635849.1:c.2168del	ENSP00000490948.1:p.Met723ArgfsTer7
ENST00000635957.1:c.1799del	ENSP00000490385.1:p.Met600ArgfsTer7
ENST00000636227.1:n.3310del
ENST00000636254.1:n.767del
ENST00000636930.2:c.4847del MANE Select	ENSP00000490491.2:p.Met1616ArgfsTer7
ENST00000636940.1:n.2844del
ENST00000637015.1:c.2215del
ENST00000637568.1:c.2129del
ENST00000637741.1:n.1513del
ENST00000637810.1:c.2189del	ENSP00000489636.1:p.Met730ArgfsTer7
ENST00000637904.1:c.2348del	ENSP00000490550.1:p.Met783ArgfsTer7
ENST00000647938.1:c.4478del	ENSP00000498155.1:p.Met1493ArgfsTer7
ENST00000346085.9:c.4478del	ENSP00000344546.4:p.Met1493ArgfsTer7
ENST00000350026.9:c.4439del	ENSP00000055163.7:p.Met1480ArgfsTer7
ENST00000414678.6:c.3005del	ENSP00000412835.2:p.Met1002ArgfsTer7
NM_017519.2:c.4439del	NP_059989.2:p.Met1480ArgfsTer7
NM_020732.3:c.4478del	NP_065783.3:p.Met1493ArgfsTer7
XM_005267069.3:c.4598del	XP_005267126.2:p.Met1533ArgfsTer7
XM_011535984.1:c.3677del	XP_011534286.1:p.Met1226ArgfsTer7
XM_011535985.1:c.3497del	XP_011534287.1:p.Met1166ArgfsTer7
XM_011535986.1:c.3257del	XP_011534288.1:p.Met1086ArgfsTer7
XM_011535987.1:c.2876del	XP_011534289.1:p.Met959ArgfsTer7
XM_011535988.1:c.1739del	XP_011534290.1:p.Met580ArgfsTer7
NM_001346813.1:c.4598del	NP_001333742.1:p.Met1533ArgfsTer7
NM_001363725.1:c.2348del	NP_001350654.1:p.Met783ArgfsTer7
XM_011535984.2:c.4808del	XP_011534286.2:p.Met1603ArgfsTer7
XM_011535988.3:c.1739del	XP_011534290.1:p.Met580ArgfsTer7
XM_017011103.2:c.4709del	XP_016866592.1:p.Met1570ArgfsTer7
XM_017011104.1:c.4679del	XP_016866593.1:p.Met1560ArgfsTer7
XM_017011105.2:c.4649del	XP_016866594.1:p.Met1550ArgfsTer7
XM_017011106.2:c.4520del	XP_016866595.1:p.Met1507ArgfsTer7
XM_017011107.2:c.4499del	XP_016866596.1:p.Met1500ArgfsTer7
XR_002956289.1:n.4794del
NM_001363725.2:c.2348del	NP_001350654.1:p.Met783ArgfsTer7
NM_001371656.1:c.4727del	NP_001358585.1:p.Met1576ArgfsTer7
NM_001374820.1:c.4727del	NP_001361749.1:p.Met1576ArgfsTer7
NM_001374828.1:c.4847del MANE Select	NP_001361757.1:p.Met1616ArgfsTer7
NM_017519.3:c.4688del	NP_059989.3:p.Met1563ArgfsTer7