Canonical Allele Identifier: CA10602935

Gene: ARID1B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206688dup , CM000668.2:g.157206688dup	GRCh38
NC_000006.11:g.157527822dup , CM000668.1:g.157527822dup	GRCh37
NC_000006.10:g.157569514dup	NCBI36
NG_032093.1:g.433759dup
NG_032093.2:g.433759dup
NG_066624.1:g.435663dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5757dup	ENSP00000055163.8:p.Ser1921LysfsTer5
ENST00000414678.8:c.5826dup	ENSP00000412835.3:p.Ser1944LysfsTer5
ENST00000637015.2:c.6045dup	ENSP00000489729.2:p.Ser2017LysfsTer5
ENST00000346085.10:c.5796dup	ENSP00000344546.5:p.Ser1934LysfsTer5
ENST00000350026.10:c.5508dup	ENSP00000055163.7:p.Ser1838LysfsTer5
ENST00000414678.7:c.4074dup	ENSP00000412835.2:p.Ser1360LysfsTer5
ENST00000635849.1:c.3237dup	ENSP00000490948.1:p.Ser1081LysfsTer5
ENST00000635928.1:c.72dup	ENSP00000489717.1:p.Ser26LysfsTer5
ENST00000635957.1:c.2868dup	ENSP00000490385.1:p.Ser958LysfsTer5
ENST00000636227.1:n.4379dup
ENST00000636254.1:n.1836dup
ENST00000636930.2:c.5916dup MANE Select	ENSP00000490491.2:p.Ser1974LysfsTer5
ENST00000636940.1:n.3913dup
ENST00000637015.1:c.3284dup
ENST00000637568.1:c.3198dup
ENST00000637741.1:n.2582dup
ENST00000637810.1:c.3258dup	ENSP00000489636.1:p.Ser1088LysfsTer5
ENST00000637904.1:c.3417dup	ENSP00000490550.1:p.Ser1141LysfsTer5
ENST00000637933.1:n.3031dup
ENST00000647938.1:c.5547dup	ENSP00000498155.1:p.Ser1851LysfsTer5
ENST00000346085.9:c.5547dup	ENSP00000344546.4:p.Ser1851LysfsTer5
ENST00000350026.9:c.5508dup	ENSP00000055163.7:p.Ser1838LysfsTer5
ENST00000414678.6:c.4074dup	ENSP00000412835.2:p.Ser1360LysfsTer5
NM_017519.2:c.5508dup	NP_059989.2:p.Ser1838LysfsTer5
NM_020732.3:c.5547dup	NP_065783.3:p.Ser1851LysfsTer5
XM_005267069.3:c.5667dup	XP_005267126.2:p.Ser1891LysfsTer5
XM_011535984.1:c.4746dup	XP_011534286.1:p.Ser1584LysfsTer5
XM_011535985.1:c.4566dup	XP_011534287.1:p.Ser1524LysfsTer5
XM_011535986.1:c.4326dup	XP_011534288.1:p.Ser1444LysfsTer5
XM_011535987.1:c.3945dup	XP_011534289.1:p.Ser1317LysfsTer5
XM_011535988.1:c.2808dup	XP_011534290.1:p.Ser938LysfsTer5
NM_001346813.1:c.5667dup	NP_001333742.1:p.Ser1891LysfsTer5
NM_001363725.1:c.3417dup	NP_001350654.1:p.Ser1141LysfsTer5
XM_011535984.2:c.5877dup	XP_011534286.2:p.Ser1961LysfsTer5
XM_011535988.3:c.2808dup	XP_011534290.1:p.Ser938LysfsTer5
XM_017011103.2:c.5778dup	XP_016866592.1:p.Ser1928LysfsTer5
XM_017011104.1:c.5748dup	XP_016866593.1:p.Ser1918LysfsTer5
XM_017011105.2:c.5718dup	XP_016866594.1:p.Ser1908LysfsTer5
XM_017011106.2:c.5589dup	XP_016866595.1:p.Ser1865LysfsTer5
XM_017011107.2:c.5568dup	XP_016866596.1:p.Ser1858LysfsTer5
XR_002956289.1:n.5863dup
NM_001363725.2:c.3417dup	NP_001350654.1:p.Ser1141LysfsTer5
NM_001371656.1:c.5796dup	NP_001358585.1:p.Ser1934LysfsTer5
NM_001374820.1:c.5796dup	NP_001361749.1:p.Ser1934LysfsTer5
NM_001374828.1:c.5916dup MANE Select	NP_001361757.1:p.Ser1974LysfsTer5
NM_017519.3:c.5757dup	NP_059989.3:p.Ser1921LysfsTer5