Canonical Allele Identifier: CA16618263

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 419490
• ClinVar RCV Id: RCV000483600 ; RCV001807257
• dbSNP Id: rs1554294674
• COSMIC: COSM3022269 ; COSM3022270 ; COSM5752820 ; COSM5752821
• MyVariant Identifiers: chr6:g.157405959dupG (hg19) ; chr6:g.157084825dupG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084825dup , CM000668.2:g.157084825dup	GRCh38
NC_000006.11:g.157405959dup , CM000668.1:g.157405959dup	GRCh37
NC_000006.10:g.157447651dup	NCBI36
NG_032093.1:g.311896dup
NG_032093.2:g.311896dup
NG_066624.1:g.313800dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2411dup	ENSP00000055163.8:p.Ser806IlefsTer27
ENST00000414678.8:c.2411dup	ENSP00000412835.3:p.Ser806IlefsTer?
ENST00000637015.2:c.2411dup	ENSP00000489729.2:p.Ser806IlefsTer27
ENST00000319584.11:c.425dup	ENSP00000313006.7:p.Ser144IlefsTer27
ENST00000346085.10:c.2450dup	ENSP00000344546.5:p.Ser819IlefsTer27
ENST00000350026.10:c.2162dup	ENSP00000055163.7:p.Ser723IlefsTer27
ENST00000414678.7:c.659dup	ENSP00000412835.2:p.Ser222IlefsTer?
ENST00000452544.2:n.312dup
ENST00000493658.2:n.60dup
ENST00000635849.1:c.-89dup	ENSP00000490948.1:n.-89dup
ENST00000636930.2:c.2411dup MANE Select	ENSP00000490491.2:p.Ser806IlefsTer27
ENST00000637003.1:c.-89dup	ENSP00000489666.1:n.-89dup
ENST00000637810.1:c.-89dup	ENSP00000489636.1:n.-89dup
ENST00000637904.1:c.-89dup	ENSP00000490550.1:n.-89dup
ENST00000647938.1:c.2201dup	ENSP00000498155.1:p.Ser736IlefsTer27
ENST00000674190.1:n.1160dup
ENST00000319584.10:c.428dup	ENSP00000313006.6:p.Ser145IlefsTer27
ENST00000346085.9:c.2201dup	ENSP00000344546.4:p.Ser736IlefsTer27
ENST00000350026.9:c.2162dup	ENSP00000055163.7:p.Ser723IlefsTer27
ENST00000414678.6:c.659dup	ENSP00000412835.2:p.Ser222IlefsTer?
ENST00000452544.1:n.270dup
ENST00000493658.1:n.60dup
NM_017519.2:c.2162dup	NP_059989.2:p.Ser723IlefsTer27
NM_020732.3:c.2201dup	NP_065783.3:p.Ser736IlefsTer27
XM_005267069.3:c.2162dup	XP_005267126.2:p.Ser723IlefsTer27
XM_011535984.1:c.1112dup	XP_011534286.1:p.Ser373IlefsTer27
XM_011535985.1:c.1112dup	XP_011534287.1:p.Ser373IlefsTer27
XM_011535986.1:c.692dup	XP_011534288.1:p.Ser233IlefsTer27
XM_011535987.1:c.311dup	XP_011534289.1:p.Ser106IlefsTer27
NM_001346813.1:c.2162dup	NP_001333742.1:p.Ser723IlefsTer27
NM_001363725.1:c.-89dup	NP_001350654.1:n.-89dup
XM_011535984.2:c.2243dup	XP_011534286.2:p.Ser750IlefsTer27
XM_017011103.2:c.2243dup	XP_016866592.1:p.Ser750IlefsTer27
XM_017011104.1:c.2243dup	XP_016866593.1:p.Ser750IlefsTer27
XM_017011105.2:c.2243dup	XP_016866594.1:p.Ser750IlefsTer27
XM_017011106.2:c.2243dup	XP_016866595.1:p.Ser750IlefsTer27
XM_017011107.2:c.2243dup	XP_016866596.1:p.Ser750IlefsTer27
XR_002956289.1:n.2326dup
NM_001363725.2:c.-89dup	NP_001350654.1:n.-89dup
NM_001371656.1:c.2450dup	NP_001358585.1:p.Ser819IlefsTer27
NM_001374820.1:c.2450dup	NP_001361749.1:p.Ser819IlefsTer27
NM_001374828.1:c.2411dup MANE Select	NP_001361757.1:p.Ser806IlefsTer27
NM_017519.3:c.2411dup	NP_059989.3:p.Ser806IlefsTer27