Canonical Allele Identifier: CA913185923

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201130_157201137del , CM000668.2:g.157201130_157201137del	GRCh38
NC_000006.11:g.157522264_157522271del , CM000668.1:g.157522264_157522271del	GRCh37
NC_000006.10:g.157563956_157563963del	NCBI36
NG_032093.1:g.428201_428208del
NG_032093.2:g.428201_428208del
NG_066624.1:g.430105_430112del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4746_4753del	ENSP00000055163.8:p.Trp1582Ter
ENST00000414678.8:c.4815_4822del	ENSP00000412835.3:p.Trp1605Ter
ENST00000637015.2:c.5034_5041del	ENSP00000489729.2:p.Trp1678Ter
ENST00000346085.10:c.4785_4792del	ENSP00000344546.5:p.Trp1595Ter
ENST00000350026.10:c.4497_4504del	ENSP00000055163.7:p.Trp1499Ter
ENST00000414678.7:c.3063_3070del	ENSP00000412835.2:p.Trp1021Ter
ENST00000635849.1:c.2226_2233del	ENSP00000490948.1:p.Trp742Ter
ENST00000635957.1:c.1857_1864del	ENSP00000490385.1:p.Trp619Ter
ENST00000636227.1:n.3368_3375del
ENST00000636254.1:n.825_832del
ENST00000636930.2:c.4905_4912del MANE Select	ENSP00000490491.2:p.Trp1635Ter
ENST00000636940.1:n.2902_2909del
ENST00000637015.1:c.2273_2280del
ENST00000637568.1:c.2187_2194del
ENST00000637741.1:n.1571_1578del
ENST00000637810.1:c.2247_2254del	ENSP00000489636.1:p.Trp749Ter
ENST00000637904.1:c.2406_2413del	ENSP00000490550.1:p.Trp802Ter
ENST00000647938.1:c.4536_4543del	ENSP00000498155.1:p.Trp1512Ter
ENST00000346085.9:c.4536_4543del	ENSP00000344546.4:p.Trp1512Ter
ENST00000350026.9:c.4497_4504del	ENSP00000055163.7:p.Trp1499Ter
ENST00000414678.6:c.3063_3070del	ENSP00000412835.2:p.Trp1021Ter
NM_017519.2:c.4497_4504del	NP_059989.2:p.Trp1499Ter
NM_020732.3:c.4536_4543del	NP_065783.3:p.Trp1512Ter
XM_005267069.3:c.4656_4663del	XP_005267126.2:p.Trp1552Ter
XM_011535984.1:c.3735_3742del	XP_011534286.1:p.Trp1245Ter
XM_011535985.1:c.3555_3562del	XP_011534287.1:p.Trp1185Ter
XM_011535986.1:c.3315_3322del	XP_011534288.1:p.Trp1105Ter
XM_011535987.1:c.2934_2941del	XP_011534289.1:p.Trp978Ter
XM_011535988.1:c.1797_1804del	XP_011534290.1:p.Trp599Ter
NM_001346813.1:c.4656_4663del	NP_001333742.1:p.Trp1552Ter
NM_001363725.1:c.2406_2413del	NP_001350654.1:p.Trp802Ter
XM_011535984.2:c.4866_4873del	XP_011534286.2:p.Trp1622Ter
XM_011535988.3:c.1797_1804del	XP_011534290.1:p.Trp599Ter
XM_017011103.2:c.4767_4774del	XP_016866592.1:p.Trp1589Ter
XM_017011104.1:c.4737_4744del	XP_016866593.1:p.Trp1579Ter
XM_017011105.2:c.4707_4714del	XP_016866594.1:p.Trp1569Ter
XM_017011106.2:c.4578_4585del	XP_016866595.1:p.Trp1526Ter
XM_017011107.2:c.4557_4564del	XP_016866596.1:p.Trp1519Ter
XR_002956289.1:n.4852_4859del
NM_001363725.2:c.2406_2413del	NP_001350654.1:p.Trp802Ter
NM_001371656.1:c.4785_4792del	NP_001358585.1:p.Trp1595Ter
NM_001374820.1:c.4785_4792del	NP_001361749.1:p.Trp1595Ter
NM_001374828.1:c.4905_4912del MANE Select	NP_001361757.1:p.Trp1635Ter
NM_017519.3:c.4746_4753del	NP_059989.3:p.Trp1582Ter