Canonical Allele Identifier: CA2580615811

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1338221
• ClinVar RCV Id: RCV001822819
• dbSNP Id: rs2128317232

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181082_157181083del , CM000668.2:g.157181082_157181083del	GRCh38
NC_000006.11:g.157502216_157502217del , CM000668.1:g.157502216_157502217del	GRCh37
NC_000006.10:g.157543908_157543909del	NCBI36
NG_032093.1:g.408153_408154del
NG_032093.2:g.408153_408154del
NG_066624.1:g.410057_410058del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3459_3460del	ENSP00000055163.8:p.Gly1154LeufsTer?
ENST00000414678.8:c.3528_3529del	ENSP00000412835.3:p.Gly1177LeufsTer?
ENST00000637015.2:c.3747_3748del	ENSP00000489729.2:p.Gly1250LeufsTer?
ENST00000319584.11:c.1632_1633del	ENSP00000313006.7:p.Gly545LeufsTer?
ENST00000346085.10:c.3498_3499del	ENSP00000344546.5:p.Gly1167LeufsTer?
ENST00000350026.10:c.3210_3211del	ENSP00000055163.7:p.Gly1071LeufsTer?
ENST00000414678.7:c.1776_1777del	ENSP00000412835.2:p.Gly593LeufsTer?
ENST00000635849.1:c.939_940del	ENSP00000490948.1:p.Gly314LeufsTer?
ENST00000635957.1:c.573_574del	ENSP00000490385.1:p.Gly192LeufsTer?
ENST00000636930.2:c.3618_3619del MANE Select	ENSP00000490491.2:p.Gly1207LeufsTer?
ENST00000636940.1:n.1615_1616del
ENST00000637015.1:c.986_987del
ENST00000637568.1:c.900_901del
ENST00000637741.1:n.284_285del
ENST00000637810.1:c.960_961del	ENSP00000489636.1:p.Gly321LeufsTer?
ENST00000637904.1:c.1119_1120del	ENSP00000490550.1:p.Gly374LeufsTer?
ENST00000647938.1:c.3249_3250del	ENSP00000498155.1:p.Gly1084LeufsTer?
ENST00000319584.10:c.1635_1636del	ENSP00000313006.6:p.Gly546LeufsTer?
ENST00000346085.9:c.3249_3250del	ENSP00000344546.4:p.Gly1084LeufsTer?
ENST00000350026.9:c.3210_3211del	ENSP00000055163.7:p.Gly1071LeufsTer?
ENST00000400790.3:c.411_412del	ENSP00000383596.3:p.Gly138LeufsTer?
ENST00000414678.6:c.1776_1777del	ENSP00000412835.2:p.Gly593LeufsTer?
ENST00000478761.3:c.820_821del
NM_017519.2:c.3210_3211del	NP_059989.2:p.Gly1071LeufsTer?
NM_020732.3:c.3249_3250del	NP_065783.3:p.Gly1084LeufsTer?
XM_005267069.3:c.3369_3370del	XP_005267126.2:p.Gly1124LeufsTer?
XM_011535984.1:c.2448_2449del	XP_011534286.1:p.Gly817LeufsTer?
XM_011535985.1:c.2268_2269del	XP_011534287.1:p.Gly757LeufsTer?
XM_011535986.1:c.2028_2029del	XP_011534288.1:p.Gly677LeufsTer?
XM_011535987.1:c.1647_1648del	XP_011534289.1:p.Gly550LeufsTer?
XM_011535988.1:c.510_511del	XP_011534290.1:p.Gly171LeufsTer?
NM_001346813.1:c.3369_3370del	NP_001333742.1:p.Gly1124LeufsTer?
NM_001363725.1:c.1119_1120del	NP_001350654.1:p.Gly374LeufsTer?
XM_011535984.2:c.3579_3580del	XP_011534286.2:p.Gly1194LeufsTer?
XM_011535988.3:c.510_511del	XP_011534290.1:p.Gly171LeufsTer?
XM_017011103.2:c.3480_3481del	XP_016866592.1:p.Gly1161LeufsTer?
XM_017011104.1:c.3450_3451del	XP_016866593.1:p.Gly1151LeufsTer?
XM_017011105.2:c.3420_3421del	XP_016866594.1:p.Gly1141LeufsTer?
XM_017011106.2:c.3291_3292del	XP_016866595.1:p.Gly1098LeufsTer?
XM_017011107.2:c.3270_3271del	XP_016866596.1:p.Gly1091LeufsTer?
XR_002956289.1:n.3662_3663del
NM_001363725.2:c.1119_1120del	NP_001350654.1:p.Gly374LeufsTer?
NM_001371656.1:c.3498_3499del	NP_001358585.1:p.Gly1167LeufsTer?
NM_001374820.1:c.3498_3499del	NP_001361749.1:p.Gly1167LeufsTer?
NM_001374828.1:c.3618_3619del MANE Select	NP_001361757.1:p.Gly1207LeufsTer?
NM_017519.3:c.3459_3460del	NP_059989.3:p.Gly1154LeufsTer?