Canonical Allele Identifier: CA2680892384

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190015-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190015_157190016insG , CM000668.2:g.157190015_157190016insG	GRCh38
NC_000006.11:g.157511149_157511150insG , CM000668.1:g.157511149_157511150insG	GRCh37
NC_000006.10:g.157552841_157552842insG	NCBI36
NG_032093.1:g.417086_417087insG
NG_032093.2:g.417086_417087insG
NG_066624.1:g.418990_418991insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3900-23_3900-22insG	ENSP00000055163.8:n.3900-23_3900-22insG
ENST00000414678.8:c.3969-23_3969-22insG	ENSP00000412835.3:n.3969-23_3969-22insG
ENST00000637015.2:c.4188-23_4188-22insG	ENSP00000489729.2:n.4188-23_4188-22insG
ENST00000346085.10:c.3939-23_3939-22insG	ENSP00000344546.5:n.3939-23_3939-22insG
ENST00000350026.10:c.3651-23_3651-22insG	ENSP00000055163.7:n.3651-23_3651-22insG
ENST00000414678.7:c.2217-23_2217-22insG	ENSP00000412835.2:n.2217-23_2217-22insG
ENST00000635849.1:c.1380-23_1380-22insG	ENSP00000490948.1:n.1380-23_1380-22insG
ENST00000635957.1:c.1014-26_1014-25insG	ENSP00000490385.1:n.1014-26_1014-25insG
ENST00000636930.2:c.4059-23_4059-22insG MANE Select	ENSP00000490491.2:n.4059-23_4059-22insG
ENST00000636940.1:n.2056-23_2056-22insG
ENST00000637015.1:c.1427-23_1427-22insG
ENST00000637568.1:c.1341-23_1341-22insG
ENST00000637741.1:n.725-23_725-22insG
ENST00000637810.1:c.1401-23_1401-22insG	ENSP00000489636.1:n.1401-23_1401-22insG
ENST00000637904.1:c.1560-23_1560-22insG	ENSP00000490550.1:n.1560-23_1560-22insG
ENST00000647938.1:c.3690-23_3690-22insG	ENSP00000498155.1:n.3690-23_3690-22insG
ENST00000346085.9:c.3690-23_3690-22insG	ENSP00000344546.4:n.3690-23_3690-22insG
ENST00000350026.9:c.3651-23_3651-22insG	ENSP00000055163.7:n.3651-23_3651-22insG
ENST00000414678.6:c.2217-23_2217-22insG	ENSP00000412835.2:n.2217-23_2217-22insG
NM_017519.2:c.3651-23_3651-22insG	NP_059989.2:n.3651-23_3651-22insG
NM_020732.3:c.3690-23_3690-22insG	NP_065783.3:n.3690-23_3690-22insG
XM_005267069.3:c.3810-23_3810-22insG	XP_005267126.2:n.3810-23_3810-22insG
XM_011535984.1:c.2889-23_2889-22insG	XP_011534286.1:n.2889-23_2889-22insG
XM_011535985.1:c.2709-23_2709-22insG	XP_011534287.1:n.2709-23_2709-22insG
XM_011535986.1:c.2469-23_2469-22insG	XP_011534288.1:n.2469-23_2469-22insG
XM_011535987.1:c.2088-23_2088-22insG	XP_011534289.1:n.2088-23_2088-22insG
XM_011535988.1:c.951-23_951-22insG	XP_011534290.1:n.951-23_951-22insG
NM_001346813.1:c.3810-23_3810-22insG	NP_001333742.1:n.3810-23_3810-22insG
NM_001363725.1:c.1560-23_1560-22insG	NP_001350654.1:n.1560-23_1560-22insG
XM_011535984.2:c.4020-23_4020-22insG	XP_011534286.2:n.4020-23_4020-22insG
XM_011535988.3:c.951-23_951-22insG	XP_011534290.1:n.951-23_951-22insG
XM_017011103.2:c.3921-23_3921-22insG	XP_016866592.1:n.3921-23_3921-22insG
XM_017011104.1:c.3891-23_3891-22insG	XP_016866593.1:n.3891-23_3891-22insG
XM_017011105.2:c.3861-23_3861-22insG	XP_016866594.1:n.3861-23_3861-22insG
XM_017011106.2:c.3732-23_3732-22insG	XP_016866595.1:n.3732-23_3732-22insG
XM_017011107.2:c.3711-23_3711-22insG	XP_016866596.1:n.3711-23_3711-22insG
XR_002956289.1:n.4103-23_4103-22insG
NM_001363725.2:c.1560-23_1560-22insG	NP_001350654.1:n.1560-23_1560-22insG
NM_001371656.1:c.3939-23_3939-22insG	NP_001358585.1:n.3939-23_3939-22insG
NM_001374820.1:c.3939-23_3939-22insG	NP_001361749.1:n.3939-23_3939-22insG
NM_001374828.1:c.4059-23_4059-22insG MANE Select	NP_001361757.1:n.4059-23_4059-22insG
NM_017519.3:c.3900-23_3900-22insG	NP_059989.3:n.3900-23_3900-22insG