Canonical Allele Identifier: CA1675538390

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190062_157190067delinsCCCATT , CM000668.2:g.157190062_157190067delinsCCCATT	GRCh38
NC_000006.11:g.157511196_157511201delinsCCCATT , CM000668.1:g.157511196_157511201delinsCCCATT	GRCh37
NC_000006.10:g.157552888_157552893delinsCCCATT	NCBI36
NG_032093.1:g.417133_417138delinsCCCATT
NG_032093.2:g.417133_417138delinsCCCATT
NG_066624.1:g.419037_419042delinsCCCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3924_3929delinsCCCATT	ENSP00000055163.8:p.Asp1308=
ENST00000414678.8:c.3993_3998delinsCCCATT	ENSP00000412835.3:p.Asp1331=
ENST00000637015.2:c.4212_4217delinsCCCATT	ENSP00000489729.2:p.Asp1404=
ENST00000346085.10:c.3963_3968delinsCCCATT	ENSP00000344546.5:p.Asp1321=
ENST00000350026.10:c.3675_3680delinsCCCATT	ENSP00000055163.7:p.Asp1225=
ENST00000414678.7:c.2241_2246delinsCCCATT	ENSP00000412835.2:p.Asp747=
ENST00000635849.1:c.1404_1409delinsCCCATT	ENSP00000490948.1:p.Asp468=
ENST00000635957.1:c.1035_1040delinsCCCATT	ENSP00000490385.1:p.Asp345=
ENST00000636930.2:c.4083_4088delinsCCCATT MANE Select	ENSP00000490491.2:p.Asp1361=
ENST00000636940.1:n.2080_2085delinsCCCATT
ENST00000637015.1:c.1451_1456delinsCCCATT
ENST00000637568.1:c.1365_1370delinsCCCATT
ENST00000637741.1:n.749_754delinsCCCATT
ENST00000637810.1:c.1425_1430delinsCCCATT	ENSP00000489636.1:p.Asp475=
ENST00000637904.1:c.1584_1589delinsCCCATT	ENSP00000490550.1:p.Asp528=
ENST00000647938.1:c.3714_3719delinsCCCATT	ENSP00000498155.1:p.Asp1238=
ENST00000346085.9:c.3714_3719delinsCCCATT	ENSP00000344546.4:p.Asp1238=
ENST00000350026.9:c.3675_3680delinsCCCATT	ENSP00000055163.7:p.Asp1225=
ENST00000414678.6:c.2241_2246delinsCCCATT	ENSP00000412835.2:p.Asp747=
NM_017519.2:c.3675_3680delinsCCCATT	NP_059989.2:p.Asp1225=
NM_020732.3:c.3714_3719delinsCCCATT	NP_065783.3:p.Asp1238=
XM_005267069.3:c.3834_3839delinsCCCATT	XP_005267126.2:p.Asp1278=
XM_011535984.1:c.2913_2918delinsCCCATT	XP_011534286.1:p.Asp971=
XM_011535985.1:c.2733_2738delinsCCCATT	XP_011534287.1:p.Asp911=
XM_011535986.1:c.2493_2498delinsCCCATT	XP_011534288.1:p.Asp831=
XM_011535987.1:c.2112_2117delinsCCCATT	XP_011534289.1:p.Asp704=
XM_011535988.1:c.975_980delinsCCCATT	XP_011534290.1:p.Asp325=
NM_001346813.1:c.3834_3839delinsCCCATT	NP_001333742.1:p.Asp1278=
NM_001363725.1:c.1584_1589delinsCCCATT	NP_001350654.1:p.Asp528=
XM_011535984.2:c.4044_4049delinsCCCATT	XP_011534286.2:p.Asp1348=
XM_011535988.3:c.975_980delinsCCCATT	XP_011534290.1:p.Asp325=
XM_017011103.2:c.3945_3950delinsCCCATT	XP_016866592.1:p.Asp1315=
XM_017011104.1:c.3915_3920delinsCCCATT	XP_016866593.1:p.Asp1305=
XM_017011105.2:c.3885_3890delinsCCCATT	XP_016866594.1:p.Asp1295=
XM_017011106.2:c.3756_3761delinsCCCATT	XP_016866595.1:p.Asp1252=
XM_017011107.2:c.3735_3740delinsCCCATT	XP_016866596.1:p.Asp1245=
XR_002956289.1:n.4127_4132delinsCCCATT
NM_001363725.2:c.1584_1589delinsCCCATT	NP_001350654.1:p.Asp528=
NM_001371656.1:c.3963_3968delinsCCCATT	NP_001358585.1:p.Asp1321=
NM_001374820.1:c.3963_3968delinsCCCATT	NP_001361749.1:p.Asp1321=
NM_001374828.1:c.4083_4088delinsCCCATT MANE Select	NP_001361757.1:p.Asp1361=
NM_017519.3:c.3924_3929delinsCCCATT	NP_059989.3:p.Asp1308=