Canonical Allele Identifier: CA2837995138

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201147_157201156dup , CM000668.2:g.157201147_157201156dup	GRCh38
NC_000006.11:g.157522281_157522290dup , CM000668.1:g.157522281_157522290dup	GRCh37
NC_000006.10:g.157563973_157563982dup	NCBI36
NG_032093.1:g.428218_428227dup
NG_032093.2:g.428218_428227dup
NG_066624.1:g.430122_430131dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4763_4772dup	ENSP00000055163.8:p.Tyr1592AlafsTer?
ENST00000414678.8:c.4832_4841dup	ENSP00000412835.3:p.Tyr1615AlafsTer?
ENST00000637015.2:c.5051_5060dup	ENSP00000489729.2:p.Tyr1688AlafsTer?
ENST00000346085.10:c.4802_4811dup	ENSP00000344546.5:p.Tyr1605AlafsTer?
ENST00000350026.10:c.4514_4523dup	ENSP00000055163.7:p.Tyr1509AlafsTer?
ENST00000414678.7:c.3080_3089dup	ENSP00000412835.2:p.Tyr1031AlafsTer?
ENST00000635849.1:c.2243_2252dup	ENSP00000490948.1:p.Tyr752AlafsTer?
ENST00000635957.1:c.1874_1883dup	ENSP00000490385.1:p.Tyr629AlafsTer?
ENST00000636227.1:n.3385_3394dup
ENST00000636254.1:n.842_851dup
ENST00000636930.2:c.4922_4931dup MANE Select	ENSP00000490491.2:p.Tyr1645AlafsTer?
ENST00000636940.1:n.2919_2928dup
ENST00000637015.1:c.2290_2299dup
ENST00000637568.1:c.2204_2213dup
ENST00000637741.1:n.1588_1597dup
ENST00000637810.1:c.2264_2273dup	ENSP00000489636.1:p.Tyr759AlafsTer?
ENST00000637904.1:c.2423_2432dup	ENSP00000490550.1:p.Tyr812AlafsTer?
ENST00000647938.1:c.4553_4562dup	ENSP00000498155.1:p.Tyr1522AlafsTer?
ENST00000346085.9:c.4553_4562dup	ENSP00000344546.4:p.Tyr1522AlafsTer?
ENST00000350026.9:c.4514_4523dup	ENSP00000055163.7:p.Tyr1509AlafsTer?
ENST00000414678.6:c.3080_3089dup	ENSP00000412835.2:p.Tyr1031AlafsTer?
NM_017519.2:c.4514_4523dup	NP_059989.2:p.Tyr1509AlafsTer?
NM_020732.3:c.4553_4562dup	NP_065783.3:p.Tyr1522AlafsTer?
XM_005267069.3:c.4673_4682dup	XP_005267126.2:p.Tyr1562AlafsTer?
XM_011535984.1:c.3752_3761dup	XP_011534286.1:p.Tyr1255AlafsTer?
XM_011535985.1:c.3572_3581dup	XP_011534287.1:p.Tyr1195AlafsTer?
XM_011535986.1:c.3332_3341dup	XP_011534288.1:p.Tyr1115AlafsTer?
XM_011535987.1:c.2951_2960dup	XP_011534289.1:p.Tyr988AlafsTer?
XM_011535988.1:c.1814_1823dup	XP_011534290.1:p.Tyr609AlafsTer?
NM_001346813.1:c.4673_4682dup	NP_001333742.1:p.Tyr1562AlafsTer?
NM_001363725.1:c.2423_2432dup	NP_001350654.1:p.Tyr812AlafsTer?
XM_011535984.2:c.4883_4892dup	XP_011534286.2:p.Tyr1632AlafsTer?
XM_011535988.3:c.1814_1823dup	XP_011534290.1:p.Tyr609AlafsTer?
XM_017011103.2:c.4784_4793dup	XP_016866592.1:p.Tyr1599AlafsTer?
XM_017011104.1:c.4754_4763dup	XP_016866593.1:p.Tyr1589AlafsTer?
XM_017011105.2:c.4724_4733dup	XP_016866594.1:p.Tyr1579AlafsTer?
XM_017011106.2:c.4595_4604dup	XP_016866595.1:p.Tyr1536AlafsTer?
XM_017011107.2:c.4574_4583dup	XP_016866596.1:p.Tyr1529AlafsTer?
XR_002956289.1:n.4869_4878dup
NM_001363725.2:c.2423_2432dup	NP_001350654.1:p.Tyr812AlafsTer?
NM_001371656.1:c.4802_4811dup	NP_001358585.1:p.Tyr1605AlafsTer?
NM_001374820.1:c.4802_4811dup	NP_001361749.1:p.Tyr1605AlafsTer?
NM_001374828.1:c.4922_4931dup MANE Select	NP_001361757.1:p.Tyr1645AlafsTer?
NM_017519.3:c.4763_4772dup	NP_059989.3:p.Tyr1592AlafsTer?