Canonical Allele Identifier: CA2773709211

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201399del , CM000668.2:g.157201399del	GRCh38
NC_000006.11:g.157522533del , CM000668.1:g.157522533del	GRCh37
NC_000006.10:g.157564225del	NCBI36
NG_032093.1:g.428470del
NG_032093.2:g.428470del
NG_066624.1:g.430374del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5015del	ENSP00000055163.8:p.Ile1672ThrfsTer12
ENST00000414678.8:c.5084del	ENSP00000412835.3:p.Ile1695ThrfsTer12
ENST00000637015.2:c.5303del	ENSP00000489729.2:p.Ile1768ThrfsTer12
ENST00000346085.10:c.5054del	ENSP00000344546.5:p.Ile1685ThrfsTer12
ENST00000350026.10:c.4766del	ENSP00000055163.7:p.Ile1589ThrfsTer12
ENST00000414678.7:c.3332del	ENSP00000412835.2:p.Ile1111ThrfsTer12
ENST00000635849.1:c.2495del	ENSP00000490948.1:p.Ile832ThrfsTer12
ENST00000635957.1:c.2126del	ENSP00000490385.1:p.Ile709ThrfsTer12
ENST00000636227.1:n.3637del
ENST00000636254.1:n.1094del
ENST00000636930.2:c.5174del MANE Select	ENSP00000490491.2:p.Ile1725ThrfsTer12
ENST00000636940.1:n.3171del
ENST00000637015.1:c.2542del
ENST00000637568.1:c.2456del
ENST00000637741.1:n.1840del
ENST00000637810.1:c.2516del	ENSP00000489636.1:p.Ile839ThrfsTer12
ENST00000637904.1:c.2675del	ENSP00000490550.1:p.Ile892ThrfsTer12
ENST00000647938.1:c.4805del	ENSP00000498155.1:p.Ile1602ThrfsTer12
ENST00000346085.9:c.4805del	ENSP00000344546.4:p.Ile1602ThrfsTer12
ENST00000350026.9:c.4766del	ENSP00000055163.7:p.Ile1589ThrfsTer12
ENST00000414678.6:c.3332del	ENSP00000412835.2:p.Ile1111ThrfsTer12
NM_017519.2:c.4766del	NP_059989.2:p.Ile1589ThrfsTer12
NM_020732.3:c.4805del	NP_065783.3:p.Ile1602ThrfsTer12
XM_005267069.3:c.4925del	XP_005267126.2:p.Ile1642ThrfsTer12
XM_011535984.1:c.4004del	XP_011534286.1:p.Ile1335ThrfsTer12
XM_011535985.1:c.3824del	XP_011534287.1:p.Ile1275ThrfsTer12
XM_011535986.1:c.3584del	XP_011534288.1:p.Ile1195ThrfsTer12
XM_011535987.1:c.3203del	XP_011534289.1:p.Ile1068ThrfsTer12
XM_011535988.1:c.2066del	XP_011534290.1:p.Ile689ThrfsTer12
NM_001346813.1:c.4925del	NP_001333742.1:p.Ile1642ThrfsTer12
NM_001363725.1:c.2675del	NP_001350654.1:p.Ile892ThrfsTer12
XM_011535984.2:c.5135del	XP_011534286.2:p.Ile1712ThrfsTer12
XM_011535988.3:c.2066del	XP_011534290.1:p.Ile689ThrfsTer12
XM_017011103.2:c.5036del	XP_016866592.1:p.Ile1679ThrfsTer12
XM_017011104.1:c.5006del	XP_016866593.1:p.Ile1669ThrfsTer12
XM_017011105.2:c.4976del	XP_016866594.1:p.Ile1659ThrfsTer12
XM_017011106.2:c.4847del	XP_016866595.1:p.Ile1616ThrfsTer12
XM_017011107.2:c.4826del	XP_016866596.1:p.Ile1609ThrfsTer12
XR_002956289.1:n.5121del
NM_001363725.2:c.2675del	NP_001350654.1:p.Ile892ThrfsTer12
NM_001371656.1:c.5054del	NP_001358585.1:p.Ile1685ThrfsTer12
NM_001374820.1:c.5054del	NP_001361749.1:p.Ile1685ThrfsTer12
NM_001374828.1:c.5174del MANE Select	NP_001361757.1:p.Ile1725ThrfsTer12
NM_017519.3:c.5015del	NP_059989.3:p.Ile1672ThrfsTer12