Canonical Allele Identifier: CA658796862

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 503938
• ClinVar RCV Id: RCV000598743
• dbSNP Id: rs1554235934

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201294_157201295delinsAGT , CM000668.2:g.157201294_157201295delinsAGT	GRCh38
NC_000006.11:g.157522428_157522429delinsAGT , CM000668.1:g.157522428_157522429delinsAGT	GRCh37
NC_000006.10:g.157564120_157564121delinsAGT	NCBI36
NG_032093.1:g.428365_428366delinsAGT
NG_032093.2:g.428365_428366delinsAGT
NG_066624.1:g.430269_430270delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4910_4911delinsAGT	ENSP00000055163.8:p.Met1637LysfsTer?
ENST00000414678.8:c.4979_4980delinsAGT	ENSP00000412835.3:p.Met1660LysfsTer?
ENST00000637015.2:c.5198_5199delinsAGT	ENSP00000489729.2:p.Met1733LysfsTer?
ENST00000346085.10:c.4949_4950delinsAGT	ENSP00000344546.5:p.Met1650LysfsTer?
ENST00000350026.10:c.4661_4662delinsAGT	ENSP00000055163.7:p.Met1554LysfsTer?
ENST00000414678.7:c.3227_3228delinsAGT	ENSP00000412835.2:p.Met1076LysfsTer?
ENST00000635849.1:c.2390_2391delinsAGT	ENSP00000490948.1:p.Met797LysfsTer?
ENST00000635957.1:c.2021_2022delinsAGT	ENSP00000490385.1:p.Met674LysfsTer?
ENST00000636227.1:n.3532_3533delinsAGT
ENST00000636254.1:n.989_990delinsAGT
ENST00000636930.2:c.5069_5070delinsAGT MANE Select	ENSP00000490491.2:p.Met1690LysfsTer?
ENST00000636940.1:n.3066_3067delinsAGT
ENST00000637015.1:c.2437_2438delinsAGT
ENST00000637568.1:c.2351_2352delinsAGT
ENST00000637741.1:n.1735_1736delinsAGT
ENST00000637810.1:c.2411_2412delinsAGT	ENSP00000489636.1:p.Met804LysfsTer?
ENST00000637904.1:c.2570_2571delinsAGT	ENSP00000490550.1:p.Met857LysfsTer?
ENST00000647938.1:c.4700_4701delinsAGT	ENSP00000498155.1:p.Met1567LysfsTer?
ENST00000346085.9:c.4700_4701delinsAGT	ENSP00000344546.4:p.Met1567LysfsTer?
ENST00000350026.9:c.4661_4662delinsAGT	ENSP00000055163.7:p.Met1554LysfsTer?
ENST00000414678.6:c.3227_3228delinsAGT	ENSP00000412835.2:p.Met1076LysfsTer?
NM_017519.2:c.4661_4662delinsAGT	NP_059989.2:p.Met1554LysfsTer?
NM_020732.3:c.4700_4701delinsAGT	NP_065783.3:p.Met1567LysfsTer?
XM_005267069.3:c.4820_4821delinsAGT	XP_005267126.2:p.Met1607LysfsTer?
XM_011535984.1:c.3899_3900delinsAGT	XP_011534286.1:p.Met1300LysfsTer?
XM_011535985.1:c.3719_3720delinsAGT	XP_011534287.1:p.Met1240LysfsTer?
XM_011535986.1:c.3479_3480delinsAGT	XP_011534288.1:p.Met1160LysfsTer?
XM_011535987.1:c.3098_3099delinsAGT	XP_011534289.1:p.Met1033LysfsTer?
XM_011535988.1:c.1961_1962delinsAGT	XP_011534290.1:p.Met654LysfsTer?
NM_001346813.1:c.4820_4821delinsAGT	NP_001333742.1:p.Met1607LysfsTer?
NM_001363725.1:c.2570_2571delinsAGT	NP_001350654.1:p.Met857LysfsTer?
XM_011535984.2:c.5030_5031delinsAGT	XP_011534286.2:p.Met1677LysfsTer?
XM_011535988.3:c.1961_1962delinsAGT	XP_011534290.1:p.Met654LysfsTer?
XM_017011103.2:c.4931_4932delinsAGT	XP_016866592.1:p.Met1644LysfsTer?
XM_017011104.1:c.4901_4902delinsAGT	XP_016866593.1:p.Met1634LysfsTer?
XM_017011105.2:c.4871_4872delinsAGT	XP_016866594.1:p.Met1624LysfsTer?
XM_017011106.2:c.4742_4743delinsAGT	XP_016866595.1:p.Met1581LysfsTer?
XM_017011107.2:c.4721_4722delinsAGT	XP_016866596.1:p.Met1574LysfsTer?
XR_002956289.1:n.5016_5017delinsAGT
NM_001363725.2:c.2570_2571delinsAGT	NP_001350654.1:p.Met857LysfsTer?
NM_001371656.1:c.4949_4950delinsAGT	NP_001358585.1:p.Met1650LysfsTer?
NM_001374820.1:c.4949_4950delinsAGT	NP_001361749.1:p.Met1650LysfsTer?
NM_001374828.1:c.5069_5070delinsAGT MANE Select	NP_001361757.1:p.Met1690LysfsTer?
NM_017519.3:c.4910_4911delinsAGT	NP_059989.3:p.Met1637LysfsTer?