Canonical Allele Identifier: CA2573140707

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206174del , CM000668.2:g.157206174del	GRCh38
NC_000006.11:g.157527308del , CM000668.1:g.157527308del	GRCh37
NC_000006.10:g.157569000del	NCBI36
NG_032093.1:g.433245del
NG_032093.2:g.433245del
NG_066624.1:g.435149del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5243del	ENSP00000055163.8:p.Gly1748AspfsTer6
ENST00000414678.8:c.5312del	ENSP00000412835.3:p.Gly1771AspfsTer6
ENST00000637015.2:c.5531del	ENSP00000489729.2:p.Gly1844AspfsTer6
ENST00000346085.10:c.5282del	ENSP00000344546.5:p.Gly1761AspfsTer6
ENST00000350026.10:c.4994del	ENSP00000055163.7:p.Gly1665AspfsTer6
ENST00000414678.7:c.3560del	ENSP00000412835.2:p.Gly1187AspfsTer6
ENST00000635849.1:c.2723del	ENSP00000490948.1:p.Gly908AspfsTer6
ENST00000635957.1:c.2354del	ENSP00000490385.1:p.Gly785AspfsTer6
ENST00000636227.1:n.3865del
ENST00000636254.1:n.1322del
ENST00000636930.2:c.5402del MANE Select	ENSP00000490491.2:p.Gly1801AspfsTer6
ENST00000636940.1:n.3399del
ENST00000637015.1:c.2770del
ENST00000637568.1:c.2684del
ENST00000637741.1:n.2068del
ENST00000637810.1:c.2744del	ENSP00000489636.1:p.Gly915AspfsTer6
ENST00000637904.1:c.2903del	ENSP00000490550.1:p.Gly968AspfsTer6
ENST00000637933.1:n.2517del
ENST00000647938.1:c.5033del	ENSP00000498155.1:p.Gly1678AspfsTer6
ENST00000346085.9:c.5033del	ENSP00000344546.4:p.Gly1678AspfsTer6
ENST00000350026.9:c.4994del	ENSP00000055163.7:p.Gly1665AspfsTer6
ENST00000414678.6:c.3560del	ENSP00000412835.2:p.Gly1187AspfsTer6
NM_017519.2:c.4994del	NP_059989.2:p.Gly1665AspfsTer6
NM_020732.3:c.5033del	NP_065783.3:p.Gly1678AspfsTer6
XM_005267069.3:c.5153del	XP_005267126.2:p.Gly1718AspfsTer6
XM_011535984.1:c.4232del	XP_011534286.1:p.Gly1411AspfsTer6
XM_011535985.1:c.4052del	XP_011534287.1:p.Gly1351AspfsTer6
XM_011535986.1:c.3812del	XP_011534288.1:p.Gly1271AspfsTer6
XM_011535987.1:c.3431del	XP_011534289.1:p.Gly1144AspfsTer6
XM_011535988.1:c.2294del	XP_011534290.1:p.Gly765AspfsTer6
NM_001346813.1:c.5153del	NP_001333742.1:p.Gly1718AspfsTer6
NM_001363725.1:c.2903del	NP_001350654.1:p.Gly968AspfsTer6
XM_011535984.2:c.5363del	XP_011534286.2:p.Gly1788AspfsTer6
XM_011535988.3:c.2294del	XP_011534290.1:p.Gly765AspfsTer6
XM_017011103.2:c.5264del	XP_016866592.1:p.Gly1755AspfsTer6
XM_017011104.1:c.5234del	XP_016866593.1:p.Gly1745AspfsTer6
XM_017011105.2:c.5204del	XP_016866594.1:p.Gly1735AspfsTer6
XM_017011106.2:c.5075del	XP_016866595.1:p.Gly1692AspfsTer6
XM_017011107.2:c.5054del	XP_016866596.1:p.Gly1685AspfsTer6
XR_002956289.1:n.5349del
NM_001363725.2:c.2903del	NP_001350654.1:p.Gly968AspfsTer6
NM_001371656.1:c.5282del	NP_001358585.1:p.Gly1761AspfsTer6
NM_001374820.1:c.5282del	NP_001361749.1:p.Gly1761AspfsTer6
NM_001374828.1:c.5402del MANE Select	NP_001361757.1:p.Gly1801AspfsTer6
NM_017519.3:c.5243del	NP_059989.3:p.Gly1748AspfsTer6