Canonical Allele Identifier: CA1675487430

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157085278_157085279delinsTG , CM000668.2:g.157085278_157085279delinsTG	GRCh38
NC_000006.11:g.157406412_157406413delinsTG , CM000668.1:g.157406412_157406413delinsTG	GRCh37
NC_000006.10:g.157448104_157448105delinsTG	NCBI36
NG_032093.1:g.312349_312350delinsTG
NG_032093.2:g.312349_312350delinsTG
NG_066624.1:g.314253_314254delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2491+373_2491+374delinsTG	ENSP00000055163.8:n.2491+373_2491+374delinsTG
ENST00000414678.8:c.2491+373_2491+374delinsTG	ENSP00000412835.3:n.2491+373_2491+374delinsTG
ENST00000637015.2:c.2491+373_2491+374delinsTG	ENSP00000489729.2:n.2491+373_2491+374delinsTG
ENST00000319584.11:c.505+373_505+374delinsTG	ENSP00000313006.7:n.505+373_505+374delinsTG
ENST00000346085.10:c.2530+373_2530+374delinsTG	ENSP00000344546.5:n.2530+373_2530+374delinsTG
ENST00000350026.10:c.2242+373_2242+374delinsTG	ENSP00000055163.7:n.2242+373_2242+374delinsTG
ENST00000414678.7:c.739+373_739+374delinsTG	ENSP00000412835.2:n.739+373_739+374delinsTG
ENST00000452544.2:n.392+373_392+374delinsTG
ENST00000493658.2:n.140+373_140+374delinsTG
ENST00000635849.1:c.-9+373_-9+374delinsTG	ENSP00000490948.1:n.-9+373_-9+374delinsTG
ENST00000636930.2:c.2491+373_2491+374delinsTG MANE Select	ENSP00000490491.2:n.2491+373_2491+374delinsTG
ENST00000637003.1:c.-9+373_-9+374delinsTG	ENSP00000489666.1:n.-9+373_-9+374delinsTG
ENST00000637810.1:c.-9+373_-9+374delinsTG	ENSP00000489636.1:n.-9+373_-9+374delinsTG
ENST00000637904.1:c.-9+373_-9+374delinsTG	ENSP00000490550.1:n.-9+373_-9+374delinsTG
ENST00000647938.1:c.2281+373_2281+374delinsTG	ENSP00000498155.1:n.2281+373_2281+374delinsTG
ENST00000674190.1:n.1240+373_1240+374delinsTG
ENST00000319584.10:c.508+373_508+374delinsTG	ENSP00000313006.6:n.508+373_508+374delinsTG
ENST00000346085.9:c.2281+373_2281+374delinsTG	ENSP00000344546.4:n.2281+373_2281+374delinsTG
ENST00000350026.9:c.2242+373_2242+374delinsTG	ENSP00000055163.7:n.2242+373_2242+374delinsTG
ENST00000414678.6:c.739+373_739+374delinsTG	ENSP00000412835.2:n.739+373_739+374delinsTG
ENST00000452544.1:n.350+373_350+374delinsTG
ENST00000493658.1:n.140+373_140+374delinsTG
NM_017519.2:c.2242+373_2242+374delinsTG	NP_059989.2:n.2242+373_2242+374delinsTG
NM_020732.3:c.2281+373_2281+374delinsTG	NP_065783.3:n.2281+373_2281+374delinsTG
XM_005267069.3:c.2242+373_2242+374delinsTG	XP_005267126.2:n.2242+373_2242+374delinsTG
XM_011535984.1:c.1192+373_1192+374delinsTG	XP_011534286.1:n.1192+373_1192+374delinsTG
XM_011535985.1:c.1192+373_1192+374delinsTG	XP_011534287.1:n.1192+373_1192+374delinsTG
XM_011535986.1:c.772+373_772+374delinsTG	XP_011534288.1:n.772+373_772+374delinsTG
XM_011535987.1:c.391+373_391+374delinsTG	XP_011534289.1:n.391+373_391+374delinsTG
NM_001346813.1:c.2242+373_2242+374delinsTG	NP_001333742.1:n.2242+373_2242+374delinsTG
NM_001363725.1:c.-9+373_-9+374delinsTG	NP_001350654.1:n.-9+373_-9+374delinsTG
XM_011535984.2:c.2323+373_2323+374delinsTG	XP_011534286.2:n.2323+373_2323+374delinsTG
XM_017011103.2:c.2323+373_2323+374delinsTG	XP_016866592.1:n.2323+373_2323+374delinsTG
XM_017011104.1:c.2323+373_2323+374delinsTG	XP_016866593.1:n.2323+373_2323+374delinsTG
XM_017011105.2:c.2323+373_2323+374delinsTG	XP_016866594.1:n.2323+373_2323+374delinsTG
XM_017011106.2:c.2323+373_2323+374delinsTG	XP_016866595.1:n.2323+373_2323+374delinsTG
XM_017011107.2:c.2323+373_2323+374delinsTG	XP_016866596.1:n.2323+373_2323+374delinsTG
XR_002956289.1:n.2406+373_2406+374delinsTG
NM_001363725.2:c.-9+373_-9+374delinsTG	NP_001350654.1:n.-9+373_-9+374delinsTG
NM_001371656.1:c.2530+373_2530+374delinsTG	NP_001358585.1:n.2530+373_2530+374delinsTG
NM_001374820.1:c.2530+373_2530+374delinsTG	NP_001361749.1:n.2530+373_2530+374delinsTG
NM_001374828.1:c.2491+373_2491+374delinsTG MANE Select	NP_001361757.1:n.2491+373_2491+374delinsTG
NM_017519.3:c.2491+373_2491+374delinsTG	NP_059989.3:n.2491+373_2491+374delinsTG