Canonical Allele Identifier: CA658821556

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 545949
• ClinVar RCV Id: RCV000657560
• dbSNP Id: rs1554235699
• MyVariant Identifiers: chr6:g.157522093del (hg19) ; chr6:g.157200959del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200959del , CM000668.2:g.157200959del	GRCh38
NC_000006.11:g.157522093del , CM000668.1:g.157522093del	GRCh37
NC_000006.10:g.157563785del	NCBI36
NG_032093.1:g.428030del
NG_032093.2:g.428030del
NG_066624.1:g.429934del

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4575del	ENSP00000055163.8:p.Ser1526ProfsTer?
ENST00000414678.8:c.4644del	ENSP00000412835.3:p.Ser1549ProfsTer?
ENST00000637015.2:c.4863del	ENSP00000489729.2:p.Ser1622ProfsTer?
ENST00000346085.10:c.4614del	ENSP00000344546.5:p.Ser1539ProfsTer?
ENST00000350026.10:c.4326del	ENSP00000055163.7:p.Ser1443ProfsTer?
ENST00000414678.7:c.2892del	ENSP00000412835.2:p.Ser965ProfsTer?
ENST00000635849.1:c.2055del	ENSP00000490948.1:p.Ser686ProfsTer?
ENST00000635957.1:c.1686del	ENSP00000490385.1:p.Ser563ProfsTer?
ENST00000636227.1:n.3197del
ENST00000636254.1:n.654del
ENST00000636930.2:c.4734del MANE Select	ENSP00000490491.2:p.Ser1579ProfsTer?
ENST00000636940.1:n.2731del
ENST00000637015.1:c.2102del
ENST00000637568.1:c.2016del
ENST00000637741.1:n.1400del
ENST00000637810.1:c.2076del	ENSP00000489636.1:p.Ser693ProfsTer?
ENST00000637904.1:c.2235del	ENSP00000490550.1:p.Ser746ProfsTer?
ENST00000647938.1:c.4365del	ENSP00000498155.1:p.Ser1456ProfsTer?
ENST00000346085.9:c.4365del	ENSP00000344546.4:p.Ser1456ProfsTer?
ENST00000350026.9:c.4326del	ENSP00000055163.7:p.Ser1443ProfsTer?
ENST00000414678.6:c.2892del	ENSP00000412835.2:p.Ser965ProfsTer?
NM_017519.2:c.4326del	NP_059989.2:p.Ser1443ProfsTer?
NM_020732.3:c.4365del	NP_065783.3:p.Ser1456ProfsTer?
XM_005267069.3:c.4485del	XP_005267126.2:p.Ser1496ProfsTer?
XM_011535984.1:c.3564del	XP_011534286.1:p.Ser1189ProfsTer?
XM_011535985.1:c.3384del	XP_011534287.1:p.Ser1129ProfsTer?
XM_011535986.1:c.3144del	XP_011534288.1:p.Ser1049ProfsTer?
XM_011535987.1:c.2763del	XP_011534289.1:p.Ser922ProfsTer?
XM_011535988.1:c.1626del	XP_011534290.1:p.Ser543ProfsTer?
NM_001346813.1:c.4485del	NP_001333742.1:p.Ser1496ProfsTer?
NM_001363725.1:c.2235del	NP_001350654.1:p.Ser746ProfsTer?
XM_011535984.2:c.4695del	XP_011534286.2:p.Ser1566ProfsTer?
XM_011535988.3:c.1626del	XP_011534290.1:p.Ser543ProfsTer?
XM_017011103.2:c.4596del	XP_016866592.1:p.Ser1533ProfsTer?
XM_017011104.1:c.4566del	XP_016866593.1:p.Ser1523ProfsTer?
XM_017011105.2:c.4536del	XP_016866594.1:p.Ser1513ProfsTer?
XM_017011106.2:c.4407del	XP_016866595.1:p.Ser1470ProfsTer?
XM_017011107.2:c.4386del	XP_016866596.1:p.Ser1463ProfsTer?
XR_002956289.1:n.4681del
NM_001363725.2:c.2235del	NP_001350654.1:p.Ser746ProfsTer?
NM_001371656.1:c.4614del	NP_001358585.1:p.Ser1539ProfsTer?
NM_001374820.1:c.4614del	NP_001361749.1:p.Ser1539ProfsTer?
NM_001374828.1:c.4734del MANE Select	NP_001361757.1:p.Ser1579ProfsTer?
NM_017519.3:c.4575del	NP_059989.3:p.Ser1526ProfsTer?