Canonical Allele Identifier: CA1675538364

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190007_157190010delinsCATT , CM000668.2:g.157190007_157190010delinsCATT	GRCh38
NC_000006.11:g.157511141_157511144delinsCATT , CM000668.1:g.157511141_157511144delinsCATT	GRCh37
NC_000006.10:g.157552833_157552836delinsCATT	NCBI36
NG_032093.1:g.417078_417081delinsCATT
NG_032093.2:g.417078_417081delinsCATT
NG_066624.1:g.418982_418985delinsCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3900-31_3900-28delinsCATT	ENSP00000055163.8:n.3900-31_3900-28delinsCATT
ENST00000414678.8:c.3969-31_3969-28delinsCATT	ENSP00000412835.3:n.3969-31_3969-28delinsCATT
ENST00000637015.2:c.4188-31_4188-28delinsCATT	ENSP00000489729.2:n.4188-31_4188-28delinsCATT
ENST00000346085.10:c.3939-31_3939-28delinsCATT	ENSP00000344546.5:n.3939-31_3939-28delinsCATT
ENST00000350026.10:c.3651-31_3651-28delinsCATT	ENSP00000055163.7:n.3651-31_3651-28delinsCATT
ENST00000414678.7:c.2217-31_2217-28delinsCATT	ENSP00000412835.2:n.2217-31_2217-28delinsCATT
ENST00000635849.1:c.1380-31_1380-28delinsCATT	ENSP00000490948.1:n.1380-31_1380-28delinsCATT
ENST00000635957.1:c.1014-34_1014-31delinsCATT	ENSP00000490385.1:n.1014-34_1014-31delinsCATT
ENST00000636930.2:c.4059-31_4059-28delinsCATT MANE Select	ENSP00000490491.2:n.4059-31_4059-28delinsCATT
ENST00000636940.1:n.2056-31_2056-28delinsCATT
ENST00000637015.1:c.1427-31_1427-28delinsCATT
ENST00000637568.1:c.1341-31_1341-28delinsCATT
ENST00000637741.1:n.725-31_725-28delinsCATT
ENST00000637810.1:c.1401-31_1401-28delinsCATT	ENSP00000489636.1:n.1401-31_1401-28delinsCATT
ENST00000637904.1:c.1560-31_1560-28delinsCATT	ENSP00000490550.1:n.1560-31_1560-28delinsCATT
ENST00000647938.1:c.3690-31_3690-28delinsCATT	ENSP00000498155.1:n.3690-31_3690-28delinsCATT
ENST00000346085.9:c.3690-31_3690-28delinsCATT	ENSP00000344546.4:n.3690-31_3690-28delinsCATT
ENST00000350026.9:c.3651-31_3651-28delinsCATT	ENSP00000055163.7:n.3651-31_3651-28delinsCATT
ENST00000414678.6:c.2217-31_2217-28delinsCATT	ENSP00000412835.2:n.2217-31_2217-28delinsCATT
NM_017519.2:c.3651-31_3651-28delinsCATT	NP_059989.2:n.3651-31_3651-28delinsCATT
NM_020732.3:c.3690-31_3690-28delinsCATT	NP_065783.3:n.3690-31_3690-28delinsCATT
XM_005267069.3:c.3810-31_3810-28delinsCATT	XP_005267126.2:n.3810-31_3810-28delinsCATT
XM_011535984.1:c.2889-31_2889-28delinsCATT	XP_011534286.1:n.2889-31_2889-28delinsCATT
XM_011535985.1:c.2709-31_2709-28delinsCATT	XP_011534287.1:n.2709-31_2709-28delinsCATT
XM_011535986.1:c.2469-31_2469-28delinsCATT	XP_011534288.1:n.2469-31_2469-28delinsCATT
XM_011535987.1:c.2088-31_2088-28delinsCATT	XP_011534289.1:n.2088-31_2088-28delinsCATT
XM_011535988.1:c.951-31_951-28delinsCATT	XP_011534290.1:n.951-31_951-28delinsCATT
NM_001346813.1:c.3810-31_3810-28delinsCATT	NP_001333742.1:n.3810-31_3810-28delinsCATT
NM_001363725.1:c.1560-31_1560-28delinsCATT	NP_001350654.1:n.1560-31_1560-28delinsCATT
XM_011535984.2:c.4020-31_4020-28delinsCATT	XP_011534286.2:n.4020-31_4020-28delinsCATT
XM_011535988.3:c.951-31_951-28delinsCATT	XP_011534290.1:n.951-31_951-28delinsCATT
XM_017011103.2:c.3921-31_3921-28delinsCATT	XP_016866592.1:n.3921-31_3921-28delinsCATT
XM_017011104.1:c.3891-31_3891-28delinsCATT	XP_016866593.1:n.3891-31_3891-28delinsCATT
XM_017011105.2:c.3861-31_3861-28delinsCATT	XP_016866594.1:n.3861-31_3861-28delinsCATT
XM_017011106.2:c.3732-31_3732-28delinsCATT	XP_016866595.1:n.3732-31_3732-28delinsCATT
XM_017011107.2:c.3711-31_3711-28delinsCATT	XP_016866596.1:n.3711-31_3711-28delinsCATT
XR_002956289.1:n.4103-31_4103-28delinsCATT
NM_001363725.2:c.1560-31_1560-28delinsCATT	NP_001350654.1:n.1560-31_1560-28delinsCATT
NM_001371656.1:c.3939-31_3939-28delinsCATT	NP_001358585.1:n.3939-31_3939-28delinsCATT
NM_001374820.1:c.3939-31_3939-28delinsCATT	NP_001361749.1:n.3939-31_3939-28delinsCATT
NM_001374828.1:c.4059-31_4059-28delinsCATT MANE Select	NP_001361757.1:n.4059-31_4059-28delinsCATT
NM_017519.3:c.3900-31_3900-28delinsCATT	NP_059989.3:n.3900-31_3900-28delinsCATT