Canonical Allele Identifier: CA2680891550

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201391-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201396dup , CM000668.2:g.157201396dup	GRCh38
NC_000006.11:g.157522530dup , CM000668.1:g.157522530dup	GRCh37
NC_000006.10:g.157564222dup	NCBI36
NG_032093.1:g.428467dup
NG_032093.2:g.428467dup
NG_066624.1:g.430371dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5012dup	ENSP00000055163.8:p.Ile1672AsnfsTer?
ENST00000414678.8:c.5081dup	ENSP00000412835.3:p.Ile1695AsnfsTer?
ENST00000637015.2:c.5300dup	ENSP00000489729.2:p.Ile1768AsnfsTer?
ENST00000346085.10:c.5051dup	ENSP00000344546.5:p.Ile1685AsnfsTer?
ENST00000350026.10:c.4763dup	ENSP00000055163.7:p.Ile1589AsnfsTer?
ENST00000414678.7:c.3329dup	ENSP00000412835.2:p.Ile1111AsnfsTer?
ENST00000635849.1:c.2492dup	ENSP00000490948.1:p.Ile832AsnfsTer?
ENST00000635957.1:c.2123dup	ENSP00000490385.1:p.Ile709AsnfsTer?
ENST00000636227.1:n.3634dup
ENST00000636254.1:n.1091dup
ENST00000636930.2:c.5171dup MANE Select	ENSP00000490491.2:p.Ile1725AsnfsTer?
ENST00000636940.1:n.3168dup
ENST00000637015.1:c.2539dup
ENST00000637568.1:c.2453dup
ENST00000637741.1:n.1837dup
ENST00000637810.1:c.2513dup	ENSP00000489636.1:p.Ile839AsnfsTer?
ENST00000637904.1:c.2672dup	ENSP00000490550.1:p.Ile892AsnfsTer?
ENST00000647938.1:c.4802dup	ENSP00000498155.1:p.Ile1602AsnfsTer?
ENST00000346085.9:c.4802dup	ENSP00000344546.4:p.Ile1602AsnfsTer?
ENST00000350026.9:c.4763dup	ENSP00000055163.7:p.Ile1589AsnfsTer?
ENST00000414678.6:c.3329dup	ENSP00000412835.2:p.Ile1111AsnfsTer?
NM_017519.2:c.4763dup	NP_059989.2:p.Ile1589AsnfsTer?
NM_020732.3:c.4802dup	NP_065783.3:p.Ile1602AsnfsTer?
XM_005267069.3:c.4922dup	XP_005267126.2:p.Ile1642AsnfsTer?
XM_011535984.1:c.4001dup	XP_011534286.1:p.Ile1335AsnfsTer?
XM_011535985.1:c.3821dup	XP_011534287.1:p.Ile1275AsnfsTer?
XM_011535986.1:c.3581dup	XP_011534288.1:p.Ile1195AsnfsTer?
XM_011535987.1:c.3200dup	XP_011534289.1:p.Ile1068AsnfsTer?
XM_011535988.1:c.2063dup	XP_011534290.1:p.Ile689AsnfsTer?
NM_001346813.1:c.4922dup	NP_001333742.1:p.Ile1642AsnfsTer?
NM_001363725.1:c.2672dup	NP_001350654.1:p.Ile892AsnfsTer?
XM_011535984.2:c.5132dup	XP_011534286.2:p.Ile1712AsnfsTer?
XM_011535988.3:c.2063dup	XP_011534290.1:p.Ile689AsnfsTer?
XM_017011103.2:c.5033dup	XP_016866592.1:p.Ile1679AsnfsTer?
XM_017011104.1:c.5003dup	XP_016866593.1:p.Ile1669AsnfsTer?
XM_017011105.2:c.4973dup	XP_016866594.1:p.Ile1659AsnfsTer?
XM_017011106.2:c.4844dup	XP_016866595.1:p.Ile1616AsnfsTer?
XM_017011107.2:c.4823dup	XP_016866596.1:p.Ile1609AsnfsTer?
XR_002956289.1:n.5118dup
NM_001363725.2:c.2672dup	NP_001350654.1:p.Ile892AsnfsTer?
NM_001371656.1:c.5051dup	NP_001358585.1:p.Ile1685AsnfsTer?
NM_001374820.1:c.5051dup	NP_001361749.1:p.Ile1685AsnfsTer?
NM_001374828.1:c.5171dup MANE Select	NP_001361757.1:p.Ile1725AsnfsTer?
NM_017519.3:c.5012dup	NP_059989.3:p.Ile1672AsnfsTer?