Canonical Allele Identifier: CA452978385

Gene: ARID1B

Linked Data

• COSMIC: COSM1658809 ; COSM1658810
• MyVariant Identifiers: chr6:g.157522172del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201039del , CM000668.2:g.157201039del	GRCh38
NC_000006.11:g.157522173del , CM000668.1:g.157522173del	GRCh37
NC_000006.10:g.157563865del	NCBI36
NG_032093.1:g.428110del
NG_032093.2:g.428110del
NG_066624.1:g.430014del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4655del	ENSP00000055163.8:p.Gly1552AlafsTer12
ENST00000414678.8:c.4724del	ENSP00000412835.3:p.Gly1575AlafsTer12
ENST00000637015.2:c.4943del	ENSP00000489729.2:p.Gly1648AlafsTer12
ENST00000346085.10:c.4694del	ENSP00000344546.5:p.Gly1565AlafsTer12
ENST00000350026.10:c.4406del	ENSP00000055163.7:p.Gly1469AlafsTer12
ENST00000414678.7:c.2972del	ENSP00000412835.2:p.Gly991AlafsTer12
ENST00000635849.1:c.2135del	ENSP00000490948.1:p.Gly712AlafsTer12
ENST00000635957.1:c.1766del	ENSP00000490385.1:p.Gly589AlafsTer12
ENST00000636227.1:n.3277del
ENST00000636254.1:n.734del
ENST00000636930.2:c.4814del MANE Select	ENSP00000490491.2:p.Gly1605AlafsTer12
ENST00000636940.1:n.2811del
ENST00000637015.1:c.2182del
ENST00000637568.1:c.2096del
ENST00000637741.1:n.1480del
ENST00000637810.1:c.2156del	ENSP00000489636.1:p.Gly719AlafsTer12
ENST00000637904.1:c.2315del	ENSP00000490550.1:p.Gly772AlafsTer12
ENST00000647938.1:c.4445del	ENSP00000498155.1:p.Gly1482AlafsTer12
ENST00000346085.9:c.4445del	ENSP00000344546.4:p.Gly1482AlafsTer12
ENST00000350026.9:c.4406del	ENSP00000055163.7:p.Gly1469AlafsTer12
ENST00000414678.6:c.2972del	ENSP00000412835.2:p.Gly991AlafsTer12
NM_017519.2:c.4406del	NP_059989.2:p.Gly1469AlafsTer12
NM_020732.3:c.4445del	NP_065783.3:p.Gly1482AlafsTer12
XM_005267069.3:c.4565del	XP_005267126.2:p.Gly1522AlafsTer12
XM_011535984.1:c.3644del	XP_011534286.1:p.Gly1215AlafsTer12
XM_011535985.1:c.3464del	XP_011534287.1:p.Gly1155AlafsTer12
XM_011535986.1:c.3224del	XP_011534288.1:p.Gly1075AlafsTer12
XM_011535987.1:c.2843del	XP_011534289.1:p.Gly948AlafsTer12
XM_011535988.1:c.1706del	XP_011534290.1:p.Gly569AlafsTer12
NM_001346813.1:c.4565del	NP_001333742.1:p.Gly1522AlafsTer12
NM_001363725.1:c.2315del	NP_001350654.1:p.Gly772AlafsTer12
XM_011535984.2:c.4775del	XP_011534286.2:p.Gly1592AlafsTer12
XM_011535988.3:c.1706del	XP_011534290.1:p.Gly569AlafsTer12
XM_017011103.2:c.4676del	XP_016866592.1:p.Gly1559AlafsTer12
XM_017011104.1:c.4646del	XP_016866593.1:p.Gly1549AlafsTer12
XM_017011105.2:c.4616del	XP_016866594.1:p.Gly1539AlafsTer12
XM_017011106.2:c.4487del	XP_016866595.1:p.Gly1496AlafsTer12
XM_017011107.2:c.4466del	XP_016866596.1:p.Gly1489AlafsTer12
XR_002956289.1:n.4761del
NM_001363725.2:c.2315del	NP_001350654.1:p.Gly772AlafsTer12
NM_001371656.1:c.4694del	NP_001358585.1:p.Gly1565AlafsTer12
NM_001374820.1:c.4694del	NP_001361749.1:p.Gly1565AlafsTer12
NM_001374828.1:c.4814del MANE Select	NP_001361757.1:p.Gly1605AlafsTer12
NM_017519.3:c.4655del	NP_059989.3:p.Gly1552AlafsTer12