Canonical Allele Identifier: CA2713416346

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376243

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201361_157201362del , CM000668.2:g.157201361_157201362del	GRCh38
NC_000006.11:g.157522495_157522496del , CM000668.1:g.157522495_157522496del	GRCh37
NC_000006.10:g.157564187_157564188del	NCBI36
NG_032093.1:g.428432_428433del
NG_032093.2:g.428432_428433del
NG_066624.1:g.430336_430337del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4977_4978del	ENSP00000055163.8:p.Ser1660ProfsTer?
ENST00000414678.8:c.5046_5047del	ENSP00000412835.3:p.Ser1683ProfsTer?
ENST00000637015.2:c.5265_5266del	ENSP00000489729.2:p.Ser1756ProfsTer?
ENST00000346085.10:c.5016_5017del	ENSP00000344546.5:p.Ser1673ProfsTer?
ENST00000350026.10:c.4728_4729del	ENSP00000055163.7:p.Ser1577ProfsTer?
ENST00000414678.7:c.3294_3295del	ENSP00000412835.2:p.Ser1099ProfsTer?
ENST00000635849.1:c.2457_2458del	ENSP00000490948.1:p.Ser820ProfsTer?
ENST00000635957.1:c.2088_2089del	ENSP00000490385.1:p.Ser697ProfsTer?
ENST00000636227.1:n.3599_3600del
ENST00000636254.1:n.1056_1057del
ENST00000636930.2:c.5136_5137del MANE Select	ENSP00000490491.2:p.Ser1713ProfsTer?
ENST00000636940.1:n.3133_3134del
ENST00000637015.1:c.2504_2505del
ENST00000637568.1:c.2418_2419del
ENST00000637741.1:n.1802_1803del
ENST00000637810.1:c.2478_2479del	ENSP00000489636.1:p.Ser827ProfsTer?
ENST00000637904.1:c.2637_2638del	ENSP00000490550.1:p.Ser880ProfsTer?
ENST00000647938.1:c.4767_4768del	ENSP00000498155.1:p.Ser1590ProfsTer?
ENST00000346085.9:c.4767_4768del	ENSP00000344546.4:p.Ser1590ProfsTer?
ENST00000350026.9:c.4728_4729del	ENSP00000055163.7:p.Ser1577ProfsTer?
ENST00000414678.6:c.3294_3295del	ENSP00000412835.2:p.Ser1099ProfsTer?
NM_017519.2:c.4728_4729del	NP_059989.2:p.Ser1577ProfsTer?
NM_020732.3:c.4767_4768del	NP_065783.3:p.Ser1590ProfsTer?
XM_005267069.3:c.4887_4888del	XP_005267126.2:p.Ser1630ProfsTer?
XM_011535984.1:c.3966_3967del	XP_011534286.1:p.Ser1323ProfsTer?
XM_011535985.1:c.3786_3787del	XP_011534287.1:p.Ser1263ProfsTer?
XM_011535986.1:c.3546_3547del	XP_011534288.1:p.Ser1183ProfsTer?
XM_011535987.1:c.3165_3166del	XP_011534289.1:p.Ser1056ProfsTer?
XM_011535988.1:c.2028_2029del	XP_011534290.1:p.Ser677ProfsTer?
NM_001346813.1:c.4887_4888del	NP_001333742.1:p.Ser1630ProfsTer?
NM_001363725.1:c.2637_2638del	NP_001350654.1:p.Ser880ProfsTer?
XM_011535984.2:c.5097_5098del	XP_011534286.2:p.Ser1700ProfsTer?
XM_011535988.3:c.2028_2029del	XP_011534290.1:p.Ser677ProfsTer?
XM_017011103.2:c.4998_4999del	XP_016866592.1:p.Ser1667ProfsTer?
XM_017011104.1:c.4968_4969del	XP_016866593.1:p.Ser1657ProfsTer?
XM_017011105.2:c.4938_4939del	XP_016866594.1:p.Ser1647ProfsTer?
XM_017011106.2:c.4809_4810del	XP_016866595.1:p.Ser1604ProfsTer?
XM_017011107.2:c.4788_4789del	XP_016866596.1:p.Ser1597ProfsTer?
XR_002956289.1:n.5083_5084del
NM_001363725.2:c.2637_2638del	NP_001350654.1:p.Ser880ProfsTer?
NM_001371656.1:c.5016_5017del	NP_001358585.1:p.Ser1673ProfsTer?
NM_001374820.1:c.5016_5017del	NP_001361749.1:p.Ser1673ProfsTer?
NM_001374828.1:c.5136_5137del MANE Select	NP_001361757.1:p.Ser1713ProfsTer?
NM_017519.3:c.4977_4978del	NP_059989.3:p.Ser1660ProfsTer?