Canonical Allele Identifier: CA2713413641

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128339084

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189776_157189777insATA , CM000668.2:g.157189776_157189777insATA	GRCh38
NC_000006.11:g.157510910_157510911insATA , CM000668.1:g.157510910_157510911insATA	GRCh37
NC_000006.10:g.157552602_157552603insATA	NCBI36
NG_032093.1:g.416847_416848insATA
NG_032093.2:g.416847_416848insATA
NG_066624.1:g.418751_418752insATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3895_3896insATA	ENSP00000055163.8:p.Gly1299delinsAspArg
ENST00000414678.8:c.3964_3965insATA	ENSP00000412835.3:p.Gly1322delinsAspArg
ENST00000637015.2:c.4183_4184insATA	ENSP00000489729.2:p.Gly1395delinsAspArg
ENST00000346085.10:c.3934_3935insATA	ENSP00000344546.5:p.Gly1312delinsAspArg
ENST00000350026.10:c.3646_3647insATA	ENSP00000055163.7:p.Gly1216delinsAspArg
ENST00000414678.7:c.2212_2213insATA	ENSP00000412835.2:p.Gly738delinsAspArg
ENST00000635849.1:c.1375_1376insATA	ENSP00000490948.1:p.Gly459delinsAspArg
ENST00000635957.1:c.1009_1010insATA	ENSP00000490385.1:p.Gly337delinsAspArg
ENST00000636930.2:c.4054_4055insATA MANE Select	ENSP00000490491.2:p.Gly1352delinsAspArg
ENST00000636940.1:n.2051_2052insATA
ENST00000637015.1:c.1422_1423insATA
ENST00000637568.1:c.1336_1337insATA
ENST00000637741.1:n.720_721insATA
ENST00000637810.1:c.1396_1397insATA	ENSP00000489636.1:p.Gly466delinsAspArg
ENST00000637904.1:c.1555_1556insATA	ENSP00000490550.1:p.Gly519delinsAspArg
ENST00000647938.1:c.3685_3686insATA	ENSP00000498155.1:p.Gly1229delinsAspArg
ENST00000346085.9:c.3685_3686insATA	ENSP00000344546.4:p.Gly1229delinsAspArg
ENST00000350026.9:c.3646_3647insATA	ENSP00000055163.7:p.Gly1216delinsAspArg
ENST00000414678.6:c.2212_2213insATA	ENSP00000412835.2:p.Gly738delinsAspArg
NM_017519.2:c.3646_3647insATA	NP_059989.2:p.Gly1216delinsAspArg
NM_020732.3:c.3685_3686insATA	NP_065783.3:p.Gly1229delinsAspArg
XM_005267069.3:c.3805_3806insATA	XP_005267126.2:p.Gly1269delinsAspArg
XM_011535984.1:c.2884_2885insATA	XP_011534286.1:p.Gly962delinsAspArg
XM_011535985.1:c.2704_2705insATA	XP_011534287.1:p.Gly902delinsAspArg
XM_011535986.1:c.2464_2465insATA	XP_011534288.1:p.Gly822delinsAspArg
XM_011535987.1:c.2083_2084insATA	XP_011534289.1:p.Gly695delinsAspArg
XM_011535988.1:c.946_947insATA	XP_011534290.1:p.Gly316delinsAspArg
NM_001346813.1:c.3805_3806insATA	NP_001333742.1:p.Gly1269delinsAspArg
NM_001363725.1:c.1555_1556insATA	NP_001350654.1:p.Gly519delinsAspArg
XM_011535984.2:c.4015_4016insATA	XP_011534286.2:p.Gly1339delinsAspArg
XM_011535988.3:c.946_947insATA	XP_011534290.1:p.Gly316delinsAspArg
XM_017011103.2:c.3916_3917insATA	XP_016866592.1:p.Gly1306delinsAspArg
XM_017011104.1:c.3886_3887insATA	XP_016866593.1:p.Gly1296delinsAspArg
XM_017011105.2:c.3856_3857insATA	XP_016866594.1:p.Gly1286delinsAspArg
XM_017011106.2:c.3727_3728insATA	XP_016866595.1:p.Gly1243delinsAspArg
XM_017011107.2:c.3706_3707insATA	XP_016866596.1:p.Gly1236delinsAspArg
XR_002956289.1:n.4098_4099insATA
NM_001363725.2:c.1555_1556insATA	NP_001350654.1:p.Gly519delinsAspArg
NM_001371656.1:c.3934_3935insATA	NP_001358585.1:p.Gly1312delinsAspArg
NM_001374820.1:c.3934_3935insATA	NP_001361749.1:p.Gly1312delinsAspArg
NM_001374828.1:c.4054_4055insATA MANE Select	NP_001361757.1:p.Gly1352delinsAspArg
NM_017519.3:c.3895_3896insATA	NP_059989.3:p.Gly1299delinsAspArg