Canonical Allele Identifier: CA658796859

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 524204
• ClinVar RCV Id: RCV000627688
• dbSNP Id: rs1554232959
• MyVariant Identifiers: chr6:g.157510857dup (hg19) ; chr6:g.157189723dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189723dup , CM000668.2:g.157189723dup	GRCh38
NC_000006.11:g.157510857dup , CM000668.1:g.157510857dup	GRCh37
NC_000006.10:g.157552549dup	NCBI36
NG_032093.1:g.416794dup
NG_032093.2:g.416794dup
NG_066624.1:g.418698dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3842dup	ENSP00000055163.8:p.Pro1282AlafsTer?
ENST00000414678.8:c.3911dup	ENSP00000412835.3:p.Pro1305AlafsTer?
ENST00000637015.2:c.4130dup	ENSP00000489729.2:p.Pro1378AlafsTer?
ENST00000346085.10:c.3881dup	ENSP00000344546.5:p.Pro1295AlafsTer?
ENST00000350026.10:c.3593dup	ENSP00000055163.7:p.Pro1199AlafsTer?
ENST00000414678.7:c.2159dup	ENSP00000412835.2:p.Pro721AlafsTer?
ENST00000635849.1:c.1322dup	ENSP00000490948.1:p.Pro442AlafsTer?
ENST00000635957.1:c.956dup	ENSP00000490385.1:p.Pro320AlafsTer?
ENST00000636930.2:c.4001dup MANE Select	ENSP00000490491.2:p.Pro1335AlafsTer?
ENST00000636940.1:n.1998dup
ENST00000637015.1:c.1369dup
ENST00000637568.1:c.1283dup
ENST00000637741.1:n.667dup
ENST00000637810.1:c.1343dup	ENSP00000489636.1:p.Pro449AlafsTer?
ENST00000637904.1:c.1502dup	ENSP00000490550.1:p.Pro502AlafsTer?
ENST00000647938.1:c.3632dup	ENSP00000498155.1:p.Pro1212AlafsTer?
ENST00000346085.9:c.3632dup	ENSP00000344546.4:p.Pro1212AlafsTer?
ENST00000350026.9:c.3593dup	ENSP00000055163.7:p.Pro1199AlafsTer?
ENST00000414678.6:c.2159dup	ENSP00000412835.2:p.Pro721AlafsTer?
NM_017519.2:c.3593dup	NP_059989.2:p.Pro1199AlafsTer?
NM_020732.3:c.3632dup	NP_065783.3:p.Pro1212AlafsTer?
XM_005267069.3:c.3752dup	XP_005267126.2:p.Pro1252AlafsTer?
XM_011535984.1:c.2831dup	XP_011534286.1:p.Pro945AlafsTer?
XM_011535985.1:c.2651dup	XP_011534287.1:p.Pro885AlafsTer?
XM_011535986.1:c.2411dup	XP_011534288.1:p.Pro805AlafsTer?
XM_011535987.1:c.2030dup	XP_011534289.1:p.Pro678AlafsTer?
XM_011535988.1:c.893dup	XP_011534290.1:p.Pro299AlafsTer?
NM_001346813.1:c.3752dup	NP_001333742.1:p.Pro1252AlafsTer?
NM_001363725.1:c.1502dup	NP_001350654.1:p.Pro502AlafsTer?
XM_011535984.2:c.3962dup	XP_011534286.2:p.Pro1322AlafsTer?
XM_011535988.3:c.893dup	XP_011534290.1:p.Pro299AlafsTer?
XM_017011103.2:c.3863dup	XP_016866592.1:p.Pro1289AlafsTer?
XM_017011104.1:c.3833dup	XP_016866593.1:p.Pro1279AlafsTer?
XM_017011105.2:c.3803dup	XP_016866594.1:p.Pro1269AlafsTer?
XM_017011106.2:c.3674dup	XP_016866595.1:p.Pro1226AlafsTer?
XM_017011107.2:c.3653dup	XP_016866596.1:p.Pro1219AlafsTer?
XR_002956289.1:n.4045dup
NM_001363725.2:c.1502dup	NP_001350654.1:p.Pro502AlafsTer?
NM_001371656.1:c.3881dup	NP_001358585.1:p.Pro1295AlafsTer?
NM_001374820.1:c.3881dup	NP_001361749.1:p.Pro1295AlafsTer?
NM_001374828.1:c.4001dup MANE Select	NP_001361757.1:p.Pro1335AlafsTer?
NM_017519.3:c.3842dup	NP_059989.3:p.Pro1282AlafsTer?