Canonical Allele Identifier: CA1675523257

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201255_157201258delinsCCAG , CM000668.2:g.157201255_157201258delinsCCAG	GRCh38
NC_000006.11:g.157522389_157522392delinsCCAG , CM000668.1:g.157522389_157522392delinsCCAG	GRCh37
NC_000006.10:g.157564081_157564084delinsCCAG	NCBI36
NG_032093.1:g.428326_428329delinsCCAG
NG_032093.2:g.428326_428329delinsCCAG
NG_066624.1:g.430230_430233delinsCCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4871_4874delinsCCAG	ENSP00000055163.8:p.Pro1624=
ENST00000414678.8:c.4940_4943delinsCCAG	ENSP00000412835.3:p.Pro1647=
ENST00000637015.2:c.5159_5162delinsCCAG	ENSP00000489729.2:p.Pro1720=
ENST00000346085.10:c.4910_4913delinsCCAG	ENSP00000344546.5:p.Pro1637=
ENST00000350026.10:c.4622_4625delinsCCAG	ENSP00000055163.7:p.Pro1541=
ENST00000414678.7:c.3188_3191delinsCCAG	ENSP00000412835.2:p.Pro1063=
ENST00000635849.1:c.2351_2354delinsCCAG	ENSP00000490948.1:p.Pro784=
ENST00000635957.1:c.1982_1985delinsCCAG	ENSP00000490385.1:p.Pro661=
ENST00000636227.1:n.3493_3496delinsCCAG
ENST00000636254.1:n.950_953delinsCCAG
ENST00000636930.2:c.5030_5033delinsCCAG MANE Select	ENSP00000490491.2:p.Pro1677=
ENST00000636940.1:n.3027_3030delinsCCAG
ENST00000637015.1:c.2398_2401delinsCCAG
ENST00000637568.1:c.2312_2315delinsCCAG
ENST00000637741.1:n.1696_1699delinsCCAG
ENST00000637810.1:c.2372_2375delinsCCAG	ENSP00000489636.1:p.Pro791=
ENST00000637904.1:c.2531_2534delinsCCAG	ENSP00000490550.1:p.Pro844=
ENST00000647938.1:c.4661_4664delinsCCAG	ENSP00000498155.1:p.Pro1554=
ENST00000346085.9:c.4661_4664delinsCCAG	ENSP00000344546.4:p.Pro1554=
ENST00000350026.9:c.4622_4625delinsCCAG	ENSP00000055163.7:p.Pro1541=
ENST00000414678.6:c.3188_3191delinsCCAG	ENSP00000412835.2:p.Pro1063=
NM_017519.2:c.4622_4625delinsCCAG	NP_059989.2:p.Pro1541=
NM_020732.3:c.4661_4664delinsCCAG	NP_065783.3:p.Pro1554=
XM_005267069.3:c.4781_4784delinsCCAG	XP_005267126.2:p.Pro1594=
XM_011535984.1:c.3860_3863delinsCCAG	XP_011534286.1:p.Pro1287=
XM_011535985.1:c.3680_3683delinsCCAG	XP_011534287.1:p.Pro1227=
XM_011535986.1:c.3440_3443delinsCCAG	XP_011534288.1:p.Pro1147=
XM_011535987.1:c.3059_3062delinsCCAG	XP_011534289.1:p.Pro1020=
XM_011535988.1:c.1922_1925delinsCCAG	XP_011534290.1:p.Pro641=
NM_001346813.1:c.4781_4784delinsCCAG	NP_001333742.1:p.Pro1594=
NM_001363725.1:c.2531_2534delinsCCAG	NP_001350654.1:p.Pro844=
XM_011535984.2:c.4991_4994delinsCCAG	XP_011534286.2:p.Pro1664=
XM_011535988.3:c.1922_1925delinsCCAG	XP_011534290.1:p.Pro641=
XM_017011103.2:c.4892_4895delinsCCAG	XP_016866592.1:p.Pro1631=
XM_017011104.1:c.4862_4865delinsCCAG	XP_016866593.1:p.Pro1621=
XM_017011105.2:c.4832_4835delinsCCAG	XP_016866594.1:p.Pro1611=
XM_017011106.2:c.4703_4706delinsCCAG	XP_016866595.1:p.Pro1568=
XM_017011107.2:c.4682_4685delinsCCAG	XP_016866596.1:p.Pro1561=
XR_002956289.1:n.4977_4980delinsCCAG
NM_001363725.2:c.2531_2534delinsCCAG	NP_001350654.1:p.Pro844=
NM_001371656.1:c.4910_4913delinsCCAG	NP_001358585.1:p.Pro1637=
NM_001374820.1:c.4910_4913delinsCCAG	NP_001361749.1:p.Pro1637=
NM_001374828.1:c.5030_5033delinsCCAG MANE Select	NP_001361757.1:p.Pro1677=
NM_017519.3:c.4871_4874delinsCCAG	NP_059989.3:p.Pro1624=