Canonical Allele Identifier: CA2695207255

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190064del , CM000668.2:g.157190064del	GRCh38
NC_000006.11:g.157511198del , CM000668.1:g.157511198del	GRCh37
NC_000006.10:g.157552890del	NCBI36
NG_032093.1:g.417135del
NG_032093.2:g.417135del
NG_066624.1:g.419039del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3926del	ENSP00000055163.8:p.Pro1309HisfsTer5
ENST00000414678.8:c.3995del	ENSP00000412835.3:p.Pro1332HisfsTer5
ENST00000637015.2:c.4214del	ENSP00000489729.2:p.Pro1405HisfsTer5
ENST00000346085.10:c.3965del	ENSP00000344546.5:p.Pro1322HisfsTer5
ENST00000350026.10:c.3677del	ENSP00000055163.7:p.Pro1226HisfsTer5
ENST00000414678.7:c.2243del	ENSP00000412835.2:p.Pro748HisfsTer5
ENST00000635849.1:c.1406del	ENSP00000490948.1:p.Pro469HisfsTer5
ENST00000635957.1:c.1037del	ENSP00000490385.1:p.Pro346HisfsTer5
ENST00000636930.2:c.4085del MANE Select	ENSP00000490491.2:p.Pro1362HisfsTer5
ENST00000636940.1:n.2082del
ENST00000637015.1:c.1453del
ENST00000637568.1:c.1367del
ENST00000637741.1:n.751del
ENST00000637810.1:c.1427del	ENSP00000489636.1:p.Pro476HisfsTer5
ENST00000637904.1:c.1586del	ENSP00000490550.1:p.Pro529HisfsTer5
ENST00000647938.1:c.3716del	ENSP00000498155.1:p.Pro1239HisfsTer5
ENST00000346085.9:c.3716del	ENSP00000344546.4:p.Pro1239HisfsTer5
ENST00000350026.9:c.3677del	ENSP00000055163.7:p.Pro1226HisfsTer5
ENST00000414678.6:c.2243del	ENSP00000412835.2:p.Pro748HisfsTer5
NM_017519.2:c.3677del	NP_059989.2:p.Pro1226HisfsTer5
NM_020732.3:c.3716del	NP_065783.3:p.Pro1239HisfsTer5
XM_005267069.3:c.3836del	XP_005267126.2:p.Pro1279HisfsTer5
XM_011535984.1:c.2915del	XP_011534286.1:p.Pro972HisfsTer5
XM_011535985.1:c.2735del	XP_011534287.1:p.Pro912HisfsTer5
XM_011535986.1:c.2495del	XP_011534288.1:p.Pro832HisfsTer5
XM_011535987.1:c.2114del	XP_011534289.1:p.Pro705HisfsTer5
XM_011535988.1:c.977del	XP_011534290.1:p.Pro326HisfsTer5
NM_001346813.1:c.3836del	NP_001333742.1:p.Pro1279HisfsTer5
NM_001363725.1:c.1586del	NP_001350654.1:p.Pro529HisfsTer5
XM_011535984.2:c.4046del	XP_011534286.2:p.Pro1349HisfsTer5
XM_011535988.3:c.977del	XP_011534290.1:p.Pro326HisfsTer5
XM_017011103.2:c.3947del	XP_016866592.1:p.Pro1316HisfsTer5
XM_017011104.1:c.3917del	XP_016866593.1:p.Pro1306HisfsTer5
XM_017011105.2:c.3887del	XP_016866594.1:p.Pro1296HisfsTer5
XM_017011106.2:c.3758del	XP_016866595.1:p.Pro1253HisfsTer5
XM_017011107.2:c.3737del	XP_016866596.1:p.Pro1246HisfsTer5
XR_002956289.1:n.4129del
NM_001363725.2:c.1586del	NP_001350654.1:p.Pro529HisfsTer5
NM_001371656.1:c.3965del	NP_001358585.1:p.Pro1322HisfsTer5
NM_001374820.1:c.3965del	NP_001361749.1:p.Pro1322HisfsTer5
NM_001374828.1:c.4085del MANE Select	NP_001361757.1:p.Pro1362HisfsTer5
NM_017519.3:c.3926del	NP_059989.3:p.Pro1309HisfsTer5