Canonical Allele Identifier: CA2838032945

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189695_157189696del , CM000668.2:g.157189695_157189696del	GRCh38
NC_000006.11:g.157510829_157510830del , CM000668.1:g.157510829_157510830del	GRCh37
NC_000006.10:g.157552521_157552522del	NCBI36
NG_032093.1:g.416766_416767del
NG_032093.2:g.416766_416767del
NG_066624.1:g.418670_418671del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3814_3815del	ENSP00000055163.8:p.Ser1272HisfsTer7
ENST00000414678.8:c.3883_3884del	ENSP00000412835.3:p.Ser1295HisfsTer7
ENST00000637015.2:c.4102_4103del	ENSP00000489729.2:p.Ser1368HisfsTer7
ENST00000346085.10:c.3853_3854del	ENSP00000344546.5:p.Ser1285HisfsTer7
ENST00000350026.10:c.3565_3566del	ENSP00000055163.7:p.Ser1189HisfsTer7
ENST00000414678.7:c.2131_2132del	ENSP00000412835.2:p.Ser711HisfsTer7
ENST00000635849.1:c.1294_1295del	ENSP00000490948.1:p.Ser432HisfsTer7
ENST00000635957.1:c.928_929del	ENSP00000490385.1:p.Ser310HisfsTer7
ENST00000636930.2:c.3973_3974del MANE Select	ENSP00000490491.2:p.Ser1325HisfsTer7
ENST00000636940.1:n.1970_1971del
ENST00000637015.1:c.1341_1342del
ENST00000637568.1:c.1255_1256del
ENST00000637741.1:n.639_640del
ENST00000637810.1:c.1315_1316del	ENSP00000489636.1:p.Ser439HisfsTer7
ENST00000637904.1:c.1474_1475del	ENSP00000490550.1:p.Ser492HisfsTer7
ENST00000647938.1:c.3604_3605del	ENSP00000498155.1:p.Ser1202HisfsTer7
ENST00000346085.9:c.3604_3605del	ENSP00000344546.4:p.Ser1202HisfsTer7
ENST00000350026.9:c.3565_3566del	ENSP00000055163.7:p.Ser1189HisfsTer7
ENST00000414678.6:c.2131_2132del	ENSP00000412835.2:p.Ser711HisfsTer7
NM_017519.2:c.3565_3566del	NP_059989.2:p.Ser1189HisfsTer7
NM_020732.3:c.3604_3605del	NP_065783.3:p.Ser1202HisfsTer7
XM_005267069.3:c.3724_3725del	XP_005267126.2:p.Ser1242HisfsTer7
XM_011535984.1:c.2803_2804del	XP_011534286.1:p.Ser935HisfsTer7
XM_011535985.1:c.2623_2624del	XP_011534287.1:p.Ser875HisfsTer7
XM_011535986.1:c.2383_2384del	XP_011534288.1:p.Ser795HisfsTer7
XM_011535987.1:c.2002_2003del	XP_011534289.1:p.Ser668HisfsTer7
XM_011535988.1:c.865_866del	XP_011534290.1:p.Ser289HisfsTer7
NM_001346813.1:c.3724_3725del	NP_001333742.1:p.Ser1242HisfsTer7
NM_001363725.1:c.1474_1475del	NP_001350654.1:p.Ser492HisfsTer7
XM_011535984.2:c.3934_3935del	XP_011534286.2:p.Ser1312HisfsTer7
XM_011535988.3:c.865_866del	XP_011534290.1:p.Ser289HisfsTer7
XM_017011103.2:c.3835_3836del	XP_016866592.1:p.Ser1279HisfsTer7
XM_017011104.1:c.3805_3806del	XP_016866593.1:p.Ser1269HisfsTer7
XM_017011105.2:c.3775_3776del	XP_016866594.1:p.Ser1259HisfsTer7
XM_017011106.2:c.3646_3647del	XP_016866595.1:p.Ser1216HisfsTer7
XM_017011107.2:c.3625_3626del	XP_016866596.1:p.Ser1209HisfsTer7
XR_002956289.1:n.4017_4018del
NM_001363725.2:c.1474_1475del	NP_001350654.1:p.Ser492HisfsTer7
NM_001371656.1:c.3853_3854del	NP_001358585.1:p.Ser1285HisfsTer7
NM_001374820.1:c.3853_3854del	NP_001361749.1:p.Ser1285HisfsTer7
NM_001374828.1:c.3973_3974del MANE Select	NP_001361757.1:p.Ser1325HisfsTer7
NM_017519.3:c.3814_3815del	NP_059989.3:p.Ser1272HisfsTer7