Canonical Allele Identifier: CA1675516876

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148454_157148456delinsCAG , CM000668.2:g.157148454_157148456delinsCAG	GRCh38
NC_000006.11:g.157469588_157469590delinsCAG , CM000668.1:g.157469588_157469590delinsCAG	GRCh37
NC_000006.10:g.157511280_157511282delinsCAG	NCBI36
NG_032093.1:g.375525_375527delinsCAG
NG_032093.2:g.375525_375527delinsCAG
NG_066624.1:g.377429_377431delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2762-170_2762-168delinsCAG	ENSP00000055163.8:n.2762-170_2762-168delinsCAG
ENST00000414678.8:c.2672-170_2672-168delinsCAG	ENSP00000412835.3:n.2672-170_2672-168delinsCAG
ENST00000637015.2:c.2762-170_2762-168delinsCAG	ENSP00000489729.2:n.2762-170_2762-168delinsCAG
ENST00000319584.11:c.776-170_776-168delinsCAG	ENSP00000313006.7:n.776-170_776-168delinsCAG
ENST00000346085.10:c.2801-170_2801-168delinsCAG	ENSP00000344546.5:n.2801-170_2801-168delinsCAG
ENST00000350026.10:c.2513-170_2513-168delinsCAG	ENSP00000055163.7:n.2513-170_2513-168delinsCAG
ENST00000414678.7:c.920-170_920-168delinsCAG	ENSP00000412835.2:n.920-170_920-168delinsCAG
ENST00000452544.2:n.663-170_663-168delinsCAG
ENST00000635849.1:c.83-170_83-168delinsCAG	ENSP00000490948.1:n.83-170_83-168delinsCAG
ENST00000636930.2:c.2762-170_2762-168delinsCAG MANE Select	ENSP00000490491.2:n.2762-170_2762-168delinsCAG
ENST00000637810.1:c.263-170_263-168delinsCAG	ENSP00000489636.1:n.263-170_263-168delinsCAG
ENST00000637904.1:c.263-170_263-168delinsCAG	ENSP00000490550.1:n.263-170_263-168delinsCAG
ENST00000647938.1:c.2552-170_2552-168delinsCAG	ENSP00000498155.1:n.2552-170_2552-168delinsCAG
ENST00000674190.1:n.1511-170_1511-168delinsCAG
ENST00000319584.10:c.779-170_779-168delinsCAG	ENSP00000313006.6:n.779-170_779-168delinsCAG
ENST00000346085.9:c.2552-170_2552-168delinsCAG	ENSP00000344546.4:n.2552-170_2552-168delinsCAG
ENST00000350026.9:c.2513-170_2513-168delinsCAG	ENSP00000055163.7:n.2513-170_2513-168delinsCAG
ENST00000414678.6:c.920-170_920-168delinsCAG	ENSP00000412835.2:n.920-170_920-168delinsCAG
ENST00000452544.1:n.609-170_609-168delinsCAG
NM_017519.2:c.2513-170_2513-168delinsCAG	NP_059989.2:n.2513-170_2513-168delinsCAG
NM_020732.3:c.2552-170_2552-168delinsCAG	NP_065783.3:n.2552-170_2552-168delinsCAG
XM_005267069.3:c.2513-170_2513-168delinsCAG	XP_005267126.2:n.2513-170_2513-168delinsCAG
XM_011535984.1:c.1463-170_1463-168delinsCAG	XP_011534286.1:n.1463-170_1463-168delinsCAG
XM_011535985.1:c.1283-170_1283-168delinsCAG	XP_011534287.1:n.1283-170_1283-168delinsCAG
XM_011535986.1:c.1043-170_1043-168delinsCAG	XP_011534288.1:n.1043-170_1043-168delinsCAG
XM_011535987.1:c.662-170_662-168delinsCAG	XP_011534289.1:n.662-170_662-168delinsCAG
XM_011535988.1:c.-20+15247_-20+15249delinsCAG	XP_011534290.1:n.-20+15247_-20+15249delinsCAG
NM_001346813.1:c.2513-170_2513-168delinsCAG	NP_001333742.1:n.2513-170_2513-168delinsCAG
NM_001363725.1:c.263-170_263-168delinsCAG	NP_001350654.1:n.263-170_263-168delinsCAG
XM_011535984.2:c.2594-170_2594-168delinsCAG	XP_011534286.2:n.2594-170_2594-168delinsCAG
XM_011535988.3:c.-20+15247_-20+15249delinsCAG	XP_011534290.1:n.-20+15247_-20+15249delinsCAG
XM_017011103.2:c.2594-170_2594-168delinsCAG	XP_016866592.1:n.2594-170_2594-168delinsCAG
XM_017011104.1:c.2594-170_2594-168delinsCAG	XP_016866593.1:n.2594-170_2594-168delinsCAG
XM_017011105.2:c.2594-170_2594-168delinsCAG	XP_016866594.1:n.2594-170_2594-168delinsCAG
XM_017011106.2:c.2594-170_2594-168delinsCAG	XP_016866595.1:n.2594-170_2594-168delinsCAG
XM_017011107.2:c.2414-170_2414-168delinsCAG	XP_016866596.1:n.2414-170_2414-168delinsCAG
XR_002956289.1:n.2677-170_2677-168delinsCAG
NM_001363725.2:c.263-170_263-168delinsCAG	NP_001350654.1:n.263-170_263-168delinsCAG
NM_001371656.1:c.2801-170_2801-168delinsCAG	NP_001358585.1:n.2801-170_2801-168delinsCAG
NM_001374820.1:c.2801-170_2801-168delinsCAG	NP_001361749.1:n.2801-170_2801-168delinsCAG
NM_001374828.1:c.2762-170_2762-168delinsCAG MANE Select	NP_001361757.1:n.2762-170_2762-168delinsCAG
NM_017519.3:c.2762-170_2762-168delinsCAG	NP_059989.3:n.2762-170_2762-168delinsCAG