Canonical Allele Identifier: CA645564746

Gene: ARID1B

Linked Data

• COSMIC: COSM290980

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201085_157201092del , CM000668.2:g.157201085_157201092del	GRCh38
NC_000006.11:g.157522219_157522226del , CM000668.1:g.157522219_157522226del	GRCh37
NC_000006.10:g.157563911_157563918del	NCBI36
NG_032093.1:g.428156_428163del
NG_032093.2:g.428156_428163del
NG_066624.1:g.430060_430067del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4701_4708del	ENSP00000055163.8:p.Asp1568GlyfsTer9
ENST00000414678.8:c.4770_4777del	ENSP00000412835.3:p.Asp1591GlyfsTer9
ENST00000637015.2:c.4989_4996del	ENSP00000489729.2:p.Asp1664GlyfsTer9
ENST00000346085.10:c.4740_4747del	ENSP00000344546.5:p.Asp1581GlyfsTer9
ENST00000350026.10:c.4452_4459del	ENSP00000055163.7:p.Asp1485GlyfsTer9
ENST00000414678.7:c.3018_3025del	ENSP00000412835.2:p.Asp1007GlyfsTer9
ENST00000635849.1:c.2181_2188del	ENSP00000490948.1:p.Asp728GlyfsTer9
ENST00000635957.1:c.1812_1819del	ENSP00000490385.1:p.Asp605GlyfsTer9
ENST00000636227.1:n.3323_3330del
ENST00000636254.1:n.780_787del
ENST00000636930.2:c.4860_4867del MANE Select	ENSP00000490491.2:p.Asp1621GlyfsTer9
ENST00000636940.1:n.2857_2864del
ENST00000637015.1:c.2228_2235del
ENST00000637568.1:c.2142_2149del
ENST00000637741.1:n.1526_1533del
ENST00000637810.1:c.2202_2209del	ENSP00000489636.1:p.Asp735GlyfsTer9
ENST00000637904.1:c.2361_2368del	ENSP00000490550.1:p.Asp788GlyfsTer9
ENST00000647938.1:c.4491_4498del	ENSP00000498155.1:p.Asp1498GlyfsTer9
ENST00000346085.9:c.4491_4498del	ENSP00000344546.4:p.Asp1498GlyfsTer9
ENST00000350026.9:c.4452_4459del	ENSP00000055163.7:p.Asp1485GlyfsTer9
ENST00000414678.6:c.3018_3025del	ENSP00000412835.2:p.Asp1007GlyfsTer9
NM_017519.2:c.4452_4459del	NP_059989.2:p.Asp1485GlyfsTer9
NM_020732.3:c.4491_4498del	NP_065783.3:p.Asp1498GlyfsTer9
XM_005267069.3:c.4611_4618del	XP_005267126.2:p.Asp1538GlyfsTer9
XM_011535984.1:c.3690_3697del	XP_011534286.1:p.Asp1231GlyfsTer9
XM_011535985.1:c.3510_3517del	XP_011534287.1:p.Asp1171GlyfsTer9
XM_011535986.1:c.3270_3277del	XP_011534288.1:p.Asp1091GlyfsTer9
XM_011535987.1:c.2889_2896del	XP_011534289.1:p.Asp964GlyfsTer9
XM_011535988.1:c.1752_1759del	XP_011534290.1:p.Asp585GlyfsTer9
NM_001346813.1:c.4611_4618del	NP_001333742.1:p.Asp1538GlyfsTer9
NM_001363725.1:c.2361_2368del	NP_001350654.1:p.Asp788GlyfsTer9
XM_011535984.2:c.4821_4828del	XP_011534286.2:p.Asp1608GlyfsTer9
XM_011535988.3:c.1752_1759del	XP_011534290.1:p.Asp585GlyfsTer9
XM_017011103.2:c.4722_4729del	XP_016866592.1:p.Asp1575GlyfsTer9
XM_017011104.1:c.4692_4699del	XP_016866593.1:p.Asp1565GlyfsTer9
XM_017011105.2:c.4662_4669del	XP_016866594.1:p.Asp1555GlyfsTer9
XM_017011106.2:c.4533_4540del	XP_016866595.1:p.Asp1512GlyfsTer9
XM_017011107.2:c.4512_4519del	XP_016866596.1:p.Asp1505GlyfsTer9
XR_002956289.1:n.4807_4814del
NM_001363725.2:c.2361_2368del	NP_001350654.1:p.Asp788GlyfsTer9
NM_001371656.1:c.4740_4747del	NP_001358585.1:p.Asp1581GlyfsTer9
NM_001374820.1:c.4740_4747del	NP_001361749.1:p.Asp1581GlyfsTer9
NM_001374828.1:c.4860_4867del MANE Select	NP_001361757.1:p.Asp1621GlyfsTer9
NM_017519.3:c.4701_4708del	NP_059989.3:p.Asp1568GlyfsTer9