Canonical Allele Identifier: CA1675538331
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189930_157189931delinsGA , CM000668.2:g.157189930_157189931delinsGA GRCh38
NC_000006.11:g.157511064_157511065delinsGA , CM000668.1:g.157511064_157511065delinsGA GRCh37
NC_000006.10:g.157552756_157552757delinsGA NCBI36
NG_032093.1:g.417001_417002delinsGA
NG_032093.2:g.417001_417002delinsGA
NG_066624.1:g.418905_418906delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3900-108_3900-107delinsGA ENSP00000055163.8:n.3900-108_3900-107delinsGA
ENST00000414678.8:c.3969-108_3969-107delinsGA ENSP00000412835.3:n.3969-108_3969-107delinsGA
ENST00000637015.2:c.4188-108_4188-107delinsGA ENSP00000489729.2:n.4188-108_4188-107delinsGA
ENST00000346085.10:c.3939-108_3939-107delinsGA ENSP00000344546.5:n.3939-108_3939-107delinsGA
ENST00000350026.10:c.3651-108_3651-107delinsGA ENSP00000055163.7:n.3651-108_3651-107delinsGA
ENST00000414678.7:c.2217-108_2217-107delinsGA ENSP00000412835.2:n.2217-108_2217-107delinsGA
ENST00000635849.1:c.1380-108_1380-107delinsGA ENSP00000490948.1:n.1380-108_1380-107delinsGA
ENST00000635957.1:c.1014-111_1014-110delinsGA ENSP00000490385.1:n.1014-111_1014-110delinsGA
ENST00000636930.2:c.4059-108_4059-107delinsGA MANE Select ENSP00000490491.2:n.4059-108_4059-107delinsGA
ENST00000636940.1:n.2056-108_2056-107delinsGA
ENST00000637015.1:c.1427-108_1427-107delinsGA
ENST00000637568.1:c.1341-108_1341-107delinsGA
ENST00000637741.1:n.725-108_725-107delinsGA
ENST00000637810.1:c.1401-108_1401-107delinsGA ENSP00000489636.1:n.1401-108_1401-107delinsGA
ENST00000637904.1:c.1560-108_1560-107delinsGA ENSP00000490550.1:n.1560-108_1560-107delinsGA
ENST00000647938.1:c.3690-108_3690-107delinsGA ENSP00000498155.1:n.3690-108_3690-107delinsGA
ENST00000346085.9:c.3690-108_3690-107delinsGA ENSP00000344546.4:n.3690-108_3690-107delinsGA
ENST00000350026.9:c.3651-108_3651-107delinsGA ENSP00000055163.7:n.3651-108_3651-107delinsGA
ENST00000414678.6:c.2217-108_2217-107delinsGA ENSP00000412835.2:n.2217-108_2217-107delinsGA
NM_017519.2:c.3651-108_3651-107delinsGA NP_059989.2:n.3651-108_3651-107delinsGA
NM_020732.3:c.3690-108_3690-107delinsGA NP_065783.3:n.3690-108_3690-107delinsGA
XM_005267069.3:c.3810-108_3810-107delinsGA XP_005267126.2:n.3810-108_3810-107delinsGA
XM_011535984.1:c.2889-108_2889-107delinsGA XP_011534286.1:n.2889-108_2889-107delinsGA
XM_011535985.1:c.2709-108_2709-107delinsGA XP_011534287.1:n.2709-108_2709-107delinsGA
XM_011535986.1:c.2469-108_2469-107delinsGA XP_011534288.1:n.2469-108_2469-107delinsGA
XM_011535987.1:c.2088-108_2088-107delinsGA XP_011534289.1:n.2088-108_2088-107delinsGA
XM_011535988.1:c.951-108_951-107delinsGA XP_011534290.1:n.951-108_951-107delinsGA
NM_001346813.1:c.3810-108_3810-107delinsGA NP_001333742.1:n.3810-108_3810-107delinsGA
NM_001363725.1:c.1560-108_1560-107delinsGA NP_001350654.1:n.1560-108_1560-107delinsGA
XM_011535984.2:c.4020-108_4020-107delinsGA XP_011534286.2:n.4020-108_4020-107delinsGA
XM_011535988.3:c.951-108_951-107delinsGA XP_011534290.1:n.951-108_951-107delinsGA
XM_017011103.2:c.3921-108_3921-107delinsGA XP_016866592.1:n.3921-108_3921-107delinsGA
XM_017011104.1:c.3891-108_3891-107delinsGA XP_016866593.1:n.3891-108_3891-107delinsGA
XM_017011105.2:c.3861-108_3861-107delinsGA XP_016866594.1:n.3861-108_3861-107delinsGA
XM_017011106.2:c.3732-108_3732-107delinsGA XP_016866595.1:n.3732-108_3732-107delinsGA
XM_017011107.2:c.3711-108_3711-107delinsGA XP_016866596.1:n.3711-108_3711-107delinsGA
XR_002956289.1:n.4103-108_4103-107delinsGA
NM_001363725.2:c.1560-108_1560-107delinsGA NP_001350654.1:n.1560-108_1560-107delinsGA
NM_001371656.1:c.3939-108_3939-107delinsGA NP_001358585.1:n.3939-108_3939-107delinsGA
NM_001374820.1:c.3939-108_3939-107delinsGA NP_001361749.1:n.3939-108_3939-107delinsGA
NM_001374828.1:c.4059-108_4059-107delinsGA MANE Select NP_001361757.1:n.4059-108_4059-107delinsGA
NM_017519.3:c.3900-108_3900-107delinsGA NP_059989.3:n.3900-108_3900-107delinsGA