Canonical Allele Identifier: CA1675538363

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189999_157190000delinsTG , CM000668.2:g.157189999_157190000delinsTG	GRCh38
NC_000006.11:g.157511133_157511134delinsTG , CM000668.1:g.157511133_157511134delinsTG	GRCh37
NC_000006.10:g.157552825_157552826delinsTG	NCBI36
NG_032093.1:g.417070_417071delinsTG
NG_032093.2:g.417070_417071delinsTG
NG_066624.1:g.418974_418975delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3900-39_3900-38delinsTG	ENSP00000055163.8:n.3900-39_3900-38delinsTG
ENST00000414678.8:c.3969-39_3969-38delinsTG	ENSP00000412835.3:n.3969-39_3969-38delinsTG
ENST00000637015.2:c.4188-39_4188-38delinsTG	ENSP00000489729.2:n.4188-39_4188-38delinsTG
ENST00000346085.10:c.3939-39_3939-38delinsTG	ENSP00000344546.5:n.3939-39_3939-38delinsTG
ENST00000350026.10:c.3651-39_3651-38delinsTG	ENSP00000055163.7:n.3651-39_3651-38delinsTG
ENST00000414678.7:c.2217-39_2217-38delinsTG	ENSP00000412835.2:n.2217-39_2217-38delinsTG
ENST00000635849.1:c.1380-39_1380-38delinsTG	ENSP00000490948.1:n.1380-39_1380-38delinsTG
ENST00000635957.1:c.1014-42_1014-41delinsTG	ENSP00000490385.1:n.1014-42_1014-41delinsTG
ENST00000636930.2:c.4059-39_4059-38delinsTG MANE Select	ENSP00000490491.2:n.4059-39_4059-38delinsTG
ENST00000636940.1:n.2056-39_2056-38delinsTG
ENST00000637015.1:c.1427-39_1427-38delinsTG
ENST00000637568.1:c.1341-39_1341-38delinsTG
ENST00000637741.1:n.725-39_725-38delinsTG
ENST00000637810.1:c.1401-39_1401-38delinsTG	ENSP00000489636.1:n.1401-39_1401-38delinsTG
ENST00000637904.1:c.1560-39_1560-38delinsTG	ENSP00000490550.1:n.1560-39_1560-38delinsTG
ENST00000647938.1:c.3690-39_3690-38delinsTG	ENSP00000498155.1:n.3690-39_3690-38delinsTG
ENST00000346085.9:c.3690-39_3690-38delinsTG	ENSP00000344546.4:n.3690-39_3690-38delinsTG
ENST00000350026.9:c.3651-39_3651-38delinsTG	ENSP00000055163.7:n.3651-39_3651-38delinsTG
ENST00000414678.6:c.2217-39_2217-38delinsTG	ENSP00000412835.2:n.2217-39_2217-38delinsTG
NM_017519.2:c.3651-39_3651-38delinsTG	NP_059989.2:n.3651-39_3651-38delinsTG
NM_020732.3:c.3690-39_3690-38delinsTG	NP_065783.3:n.3690-39_3690-38delinsTG
XM_005267069.3:c.3810-39_3810-38delinsTG	XP_005267126.2:n.3810-39_3810-38delinsTG
XM_011535984.1:c.2889-39_2889-38delinsTG	XP_011534286.1:n.2889-39_2889-38delinsTG
XM_011535985.1:c.2709-39_2709-38delinsTG	XP_011534287.1:n.2709-39_2709-38delinsTG
XM_011535986.1:c.2469-39_2469-38delinsTG	XP_011534288.1:n.2469-39_2469-38delinsTG
XM_011535987.1:c.2088-39_2088-38delinsTG	XP_011534289.1:n.2088-39_2088-38delinsTG
XM_011535988.1:c.951-39_951-38delinsTG	XP_011534290.1:n.951-39_951-38delinsTG
NM_001346813.1:c.3810-39_3810-38delinsTG	NP_001333742.1:n.3810-39_3810-38delinsTG
NM_001363725.1:c.1560-39_1560-38delinsTG	NP_001350654.1:n.1560-39_1560-38delinsTG
XM_011535984.2:c.4020-39_4020-38delinsTG	XP_011534286.2:n.4020-39_4020-38delinsTG
XM_011535988.3:c.951-39_951-38delinsTG	XP_011534290.1:n.951-39_951-38delinsTG
XM_017011103.2:c.3921-39_3921-38delinsTG	XP_016866592.1:n.3921-39_3921-38delinsTG
XM_017011104.1:c.3891-39_3891-38delinsTG	XP_016866593.1:n.3891-39_3891-38delinsTG
XM_017011105.2:c.3861-39_3861-38delinsTG	XP_016866594.1:n.3861-39_3861-38delinsTG
XM_017011106.2:c.3732-39_3732-38delinsTG	XP_016866595.1:n.3732-39_3732-38delinsTG
XM_017011107.2:c.3711-39_3711-38delinsTG	XP_016866596.1:n.3711-39_3711-38delinsTG
XR_002956289.1:n.4103-39_4103-38delinsTG
NM_001363725.2:c.1560-39_1560-38delinsTG	NP_001350654.1:n.1560-39_1560-38delinsTG
NM_001371656.1:c.3939-39_3939-38delinsTG	NP_001358585.1:n.3939-39_3939-38delinsTG
NM_001374820.1:c.3939-39_3939-38delinsTG	NP_001361749.1:n.3939-39_3939-38delinsTG
NM_001374828.1:c.4059-39_4059-38delinsTG MANE Select	NP_001361757.1:n.4059-39_4059-38delinsTG
NM_017519.3:c.3900-39_3900-38delinsTG	NP_059989.3:n.3900-39_3900-38delinsTG