Canonical Allele Identifier: CA2580075286

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207707del , CM000668.2:g.157207707del	GRCh38
NC_000006.11:g.157528841del , CM000668.1:g.157528841del	GRCh37
NC_000006.10:g.157570533del	NCBI36
NG_032093.1:g.434778del
NG_032093.2:g.434778del
NG_066624.1:g.436682del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.6776del	ENSP00000055163.8:p.Pro2259HisfsTer4
ENST00000414678.8:c.6845del	ENSP00000412835.3:p.Pro2282HisfsTer4
ENST00000637015.2:c.7064del	ENSP00000489729.2:p.Pro2355HisfsTer4
ENST00000346085.10:c.6815del	ENSP00000344546.5:p.Pro2272HisfsTer4
ENST00000350026.10:c.6527del	ENSP00000055163.7:p.Pro2176HisfsTer4
ENST00000414678.7:c.5093del	ENSP00000412835.2:p.Pro1698HisfsTer4
ENST00000635849.1:c.4256del	ENSP00000490948.1:p.Pro1419HisfsTer4
ENST00000635928.1:c.875+216del	ENSP00000489717.1:n.875+216del
ENST00000635957.1:c.3887del	ENSP00000490385.1:p.Pro1296HisfsTer4
ENST00000636227.1:n.5398del
ENST00000636254.1:n.2855del
ENST00000636930.2:c.6935del MANE Select	ENSP00000490491.2:p.Pro2312HisfsTer4
ENST00000636940.1:n.4932del
ENST00000637015.1:c.4303del
ENST00000637568.1:c.4217del
ENST00000637741.1:n.3601del
ENST00000637810.1:c.4277del	ENSP00000489636.1:p.Pro1426HisfsTer4
ENST00000637904.1:c.4436del	ENSP00000490550.1:p.Pro1479HisfsTer4
ENST00000637933.1:n.4050del
ENST00000647938.1:c.6566del	ENSP00000498155.1:p.Pro2189HisfsTer4
ENST00000346085.9:c.6566del	ENSP00000344546.4:p.Pro2189HisfsTer4
ENST00000350026.9:c.6527del	ENSP00000055163.7:p.Pro2176HisfsTer4
ENST00000414678.6:c.5093del	ENSP00000412835.2:p.Pro1698HisfsTer4
NM_017519.2:c.6527del	NP_059989.2:p.Pro2176HisfsTer4
NM_020732.3:c.6566del	NP_065783.3:p.Pro2189HisfsTer4
XM_005267069.3:c.6686del	XP_005267126.2:p.Pro2229HisfsTer4
XM_011535984.1:c.5765del	XP_011534286.1:p.Pro1922HisfsTer4
XM_011535985.1:c.5585del	XP_011534287.1:p.Pro1862HisfsTer4
XM_011535986.1:c.5345del	XP_011534288.1:p.Pro1782HisfsTer4
XM_011535987.1:c.4964del	XP_011534289.1:p.Pro1655HisfsTer4
XM_011535988.1:c.3827del	XP_011534290.1:p.Pro1276HisfsTer4
NM_001346813.1:c.6686del	NP_001333742.1:p.Pro2229HisfsTer4
NM_001363725.1:c.4436del	NP_001350654.1:p.Pro1479HisfsTer4
XM_011535984.2:c.6896del	XP_011534286.2:p.Pro2299HisfsTer4
XM_011535988.3:c.3827del	XP_011534290.1:p.Pro1276HisfsTer4
XM_017011103.2:c.6797del	XP_016866592.1:p.Pro2266HisfsTer4
XM_017011104.1:c.6767del	XP_016866593.1:p.Pro2256HisfsTer4
XM_017011105.2:c.6737del	XP_016866594.1:p.Pro2246HisfsTer4
XM_017011106.2:c.6608del	XP_016866595.1:p.Pro2203HisfsTer4
XM_017011107.2:c.6587del	XP_016866596.1:p.Pro2196HisfsTer4
XR_002956289.1:n.6882del
NM_001363725.2:c.4436del	NP_001350654.1:p.Pro1479HisfsTer4
NM_001371656.1:c.6815del	NP_001358585.1:p.Pro2272HisfsTer4
NM_001374820.1:c.6815del	NP_001361749.1:p.Pro2272HisfsTer4
NM_001374828.1:c.6935del MANE Select	NP_001361757.1:p.Pro2312HisfsTer4
NM_017519.3:c.6776del	NP_059989.3:p.Pro2259HisfsTer4