Canonical Allele Identifier: CA2695198382

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2664992
• ClinVar RCV Id: RCV003448542

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148621_157148622delinsAG , CM000668.2:g.157148621_157148622delinsAG	GRCh38
NC_000006.11:g.157469755_157469756delinsAG , CM000668.1:g.157469755_157469756delinsAG	GRCh37
NC_000006.10:g.157511447_157511448delinsAG	NCBI36
NG_032093.1:g.375692_375693delinsAG
NG_032093.2:g.375692_375693delinsAG
NG_066624.1:g.377596_377597delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2762-3_2762-2delinsAG	ENSP00000055163.8:n.2762-3_2762-2delinsAG
ENST00000414678.8:c.2672-3_2672-2delinsAG	ENSP00000412835.3:n.2672-3_2672-2delinsAG
ENST00000637015.2:c.2762-3_2762-2delinsAG	ENSP00000489729.2:n.2762-3_2762-2delinsAG
ENST00000319584.11:c.776-3_776-2delinsAG	ENSP00000313006.7:n.776-3_776-2delinsAG
ENST00000346085.10:c.2801-3_2801-2delinsAG	ENSP00000344546.5:n.2801-3_2801-2delinsAG
ENST00000350026.10:c.2513-3_2513-2delinsAG	ENSP00000055163.7:n.2513-3_2513-2delinsAG
ENST00000414678.7:c.920-3_920-2delinsAG	ENSP00000412835.2:n.920-3_920-2delinsAG
ENST00000452544.2:n.663-3_663-2delinsAG
ENST00000635849.1:c.83-3_83-2delinsAG	ENSP00000490948.1:n.83-3_83-2delinsAG
ENST00000636930.2:c.2762-3_2762-2delinsAG MANE Select	ENSP00000490491.2:n.2762-3_2762-2delinsAG
ENST00000637810.1:c.263-3_263-2delinsAG	ENSP00000489636.1:n.263-3_263-2delinsAG
ENST00000637904.1:c.263-3_263-2delinsAG	ENSP00000490550.1:n.263-3_263-2delinsAG
ENST00000647938.1:c.2552-3_2552-2delinsAG	ENSP00000498155.1:n.2552-3_2552-2delinsAG
ENST00000674190.1:n.1511-3_1511-2delinsAG
ENST00000319584.10:c.779-3_779-2delinsAG	ENSP00000313006.6:n.779-3_779-2delinsAG
ENST00000346085.9:c.2552-3_2552-2delinsAG	ENSP00000344546.4:n.2552-3_2552-2delinsAG
ENST00000350026.9:c.2513-3_2513-2delinsAG	ENSP00000055163.7:n.2513-3_2513-2delinsAG
ENST00000414678.6:c.920-3_920-2delinsAG	ENSP00000412835.2:n.920-3_920-2delinsAG
ENST00000452544.1:n.609-3_609-2delinsAG
NM_017519.2:c.2513-3_2513-2delinsAG	NP_059989.2:n.2513-3_2513-2delinsAG
NM_020732.3:c.2552-3_2552-2delinsAG	NP_065783.3:n.2552-3_2552-2delinsAG
XM_005267069.3:c.2513-3_2513-2delinsAG	XP_005267126.2:n.2513-3_2513-2delinsAG
XM_011535984.1:c.1463-3_1463-2delinsAG	XP_011534286.1:n.1463-3_1463-2delinsAG
XM_011535985.1:c.1283-3_1283-2delinsAG	XP_011534287.1:n.1283-3_1283-2delinsAG
XM_011535986.1:c.1043-3_1043-2delinsAG	XP_011534288.1:n.1043-3_1043-2delinsAG
XM_011535987.1:c.662-3_662-2delinsAG	XP_011534289.1:n.662-3_662-2delinsAG
XM_011535988.1:c.-20+15414_-20+15415delinsAG	XP_011534290.1:n.-20+15414_-20+15415delinsAG
NM_001346813.1:c.2513-3_2513-2delinsAG	NP_001333742.1:n.2513-3_2513-2delinsAG
NM_001363725.1:c.263-3_263-2delinsAG	NP_001350654.1:n.263-3_263-2delinsAG
XM_011535984.2:c.2594-3_2594-2delinsAG	XP_011534286.2:n.2594-3_2594-2delinsAG
XM_011535988.3:c.-20+15414_-20+15415delinsAG	XP_011534290.1:n.-20+15414_-20+15415delinsAG
XM_017011103.2:c.2594-3_2594-2delinsAG	XP_016866592.1:n.2594-3_2594-2delinsAG
XM_017011104.1:c.2594-3_2594-2delinsAG	XP_016866593.1:n.2594-3_2594-2delinsAG
XM_017011105.2:c.2594-3_2594-2delinsAG	XP_016866594.1:n.2594-3_2594-2delinsAG
XM_017011106.2:c.2594-3_2594-2delinsAG	XP_016866595.1:n.2594-3_2594-2delinsAG
XM_017011107.2:c.2414-3_2414-2delinsAG	XP_016866596.1:n.2414-3_2414-2delinsAG
XR_002956289.1:n.2677-3_2677-2delinsAG
NM_001363725.2:c.263-3_263-2delinsAG	NP_001350654.1:n.263-3_263-2delinsAG
NM_001371656.1:c.2801-3_2801-2delinsAG	NP_001358585.1:n.2801-3_2801-2delinsAG
NM_001374820.1:c.2801-3_2801-2delinsAG	NP_001361749.1:n.2801-3_2801-2delinsAG
NM_001374828.1:c.2762-3_2762-2delinsAG MANE Select	NP_001361757.1:n.2762-3_2762-2delinsAG
NM_017519.3:c.2762-3_2762-2delinsAG	NP_059989.3:n.2762-3_2762-2delinsAG