Canonical Allele Identifier: CA1675516878

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148455_157148456delinsAG , CM000668.2:g.157148455_157148456delinsAG	GRCh38
NC_000006.11:g.157469589_157469590delinsAG , CM000668.1:g.157469589_157469590delinsAG	GRCh37
NC_000006.10:g.157511281_157511282delinsAG	NCBI36
NG_032093.1:g.375526_375527delinsAG
NG_032093.2:g.375526_375527delinsAG
NG_066624.1:g.377430_377431delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2762-169_2762-168delinsAG	ENSP00000055163.8:n.2762-169_2762-168delinsAG
ENST00000414678.8:c.2672-169_2672-168delinsAG	ENSP00000412835.3:n.2672-169_2672-168delinsAG
ENST00000637015.2:c.2762-169_2762-168delinsAG	ENSP00000489729.2:n.2762-169_2762-168delinsAG
ENST00000319584.11:c.776-169_776-168delinsAG	ENSP00000313006.7:n.776-169_776-168delinsAG
ENST00000346085.10:c.2801-169_2801-168delinsAG	ENSP00000344546.5:n.2801-169_2801-168delinsAG
ENST00000350026.10:c.2513-169_2513-168delinsAG	ENSP00000055163.7:n.2513-169_2513-168delinsAG
ENST00000414678.7:c.920-169_920-168delinsAG	ENSP00000412835.2:n.920-169_920-168delinsAG
ENST00000452544.2:n.663-169_663-168delinsAG
ENST00000635849.1:c.83-169_83-168delinsAG	ENSP00000490948.1:n.83-169_83-168delinsAG
ENST00000636930.2:c.2762-169_2762-168delinsAG MANE Select	ENSP00000490491.2:n.2762-169_2762-168delinsAG
ENST00000637810.1:c.263-169_263-168delinsAG	ENSP00000489636.1:n.263-169_263-168delinsAG
ENST00000637904.1:c.263-169_263-168delinsAG	ENSP00000490550.1:n.263-169_263-168delinsAG
ENST00000647938.1:c.2552-169_2552-168delinsAG	ENSP00000498155.1:n.2552-169_2552-168delinsAG
ENST00000674190.1:n.1511-169_1511-168delinsAG
ENST00000319584.10:c.779-169_779-168delinsAG	ENSP00000313006.6:n.779-169_779-168delinsAG
ENST00000346085.9:c.2552-169_2552-168delinsAG	ENSP00000344546.4:n.2552-169_2552-168delinsAG
ENST00000350026.9:c.2513-169_2513-168delinsAG	ENSP00000055163.7:n.2513-169_2513-168delinsAG
ENST00000414678.6:c.920-169_920-168delinsAG	ENSP00000412835.2:n.920-169_920-168delinsAG
ENST00000452544.1:n.609-169_609-168delinsAG
NM_017519.2:c.2513-169_2513-168delinsAG	NP_059989.2:n.2513-169_2513-168delinsAG
NM_020732.3:c.2552-169_2552-168delinsAG	NP_065783.3:n.2552-169_2552-168delinsAG
XM_005267069.3:c.2513-169_2513-168delinsAG	XP_005267126.2:n.2513-169_2513-168delinsAG
XM_011535984.1:c.1463-169_1463-168delinsAG	XP_011534286.1:n.1463-169_1463-168delinsAG
XM_011535985.1:c.1283-169_1283-168delinsAG	XP_011534287.1:n.1283-169_1283-168delinsAG
XM_011535986.1:c.1043-169_1043-168delinsAG	XP_011534288.1:n.1043-169_1043-168delinsAG
XM_011535987.1:c.662-169_662-168delinsAG	XP_011534289.1:n.662-169_662-168delinsAG
XM_011535988.1:c.-20+15248_-20+15249delinsAG	XP_011534290.1:n.-20+15248_-20+15249delinsAG
NM_001346813.1:c.2513-169_2513-168delinsAG	NP_001333742.1:n.2513-169_2513-168delinsAG
NM_001363725.1:c.263-169_263-168delinsAG	NP_001350654.1:n.263-169_263-168delinsAG
XM_011535984.2:c.2594-169_2594-168delinsAG	XP_011534286.2:n.2594-169_2594-168delinsAG
XM_011535988.3:c.-20+15248_-20+15249delinsAG	XP_011534290.1:n.-20+15248_-20+15249delinsAG
XM_017011103.2:c.2594-169_2594-168delinsAG	XP_016866592.1:n.2594-169_2594-168delinsAG
XM_017011104.1:c.2594-169_2594-168delinsAG	XP_016866593.1:n.2594-169_2594-168delinsAG
XM_017011105.2:c.2594-169_2594-168delinsAG	XP_016866594.1:n.2594-169_2594-168delinsAG
XM_017011106.2:c.2594-169_2594-168delinsAG	XP_016866595.1:n.2594-169_2594-168delinsAG
XM_017011107.2:c.2414-169_2414-168delinsAG	XP_016866596.1:n.2414-169_2414-168delinsAG
XR_002956289.1:n.2677-169_2677-168delinsAG
NM_001363725.2:c.263-169_263-168delinsAG	NP_001350654.1:n.263-169_263-168delinsAG
NM_001371656.1:c.2801-169_2801-168delinsAG	NP_001358585.1:n.2801-169_2801-168delinsAG
NM_001374820.1:c.2801-169_2801-168delinsAG	NP_001361749.1:n.2801-169_2801-168delinsAG
NM_001374828.1:c.2762-169_2762-168delinsAG MANE Select	NP_001361757.1:n.2762-169_2762-168delinsAG
NM_017519.3:c.2762-169_2762-168delinsAG	NP_059989.3:n.2762-169_2762-168delinsAG