Canonical Allele Identifier: CA2680891083

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201128-T-TGGTCTTCTCACGTCAGCCAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201130_157201131insTCTTCTCACGTCAGCCAGCGG , CM000668.2:g.157201130_157201131insTCTTCTCACGTCAGCCAGCGG	GRCh38
NC_000006.11:g.157522264_157522265insTCTTCTCACGTCAGCCAGCGG , CM000668.1:g.157522264_157522265insTCTTCTCACGTCAGCCAGCGG	GRCh37
NC_000006.10:g.157563956_157563957insTCTTCTCACGTCAGCCAGCGG	NCBI36
NG_032093.1:g.428201_428202insTCTTCTCACGTCAGCCAGCGG
NG_032093.2:g.428201_428202insTCTTCTCACGTCAGCCAGCGG
NG_066624.1:g.430105_430106insTCTTCTCACGTCAGCCAGCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4746_4747insTCTTCTCACGTCAGCCAGCGG	ENSP00000055163.8:p.Trp1582_Pro1583insSerSerHisValSerGlnArg
ENST00000414678.8:c.4815_4816insTCTTCTCACGTCAGCCAGCGG	ENSP00000412835.3:p.Trp1605_Pro1606insSerSerHisValSerGlnArg
ENST00000637015.2:c.5034_5035insTCTTCTCACGTCAGCCAGCGG	ENSP00000489729.2:p.Trp1678_Pro1679insSerSerHisValSerGlnArg
ENST00000346085.10:c.4785_4786insTCTTCTCACGTCAGCCAGCGG	ENSP00000344546.5:p.Trp1595_Pro1596insSerSerHisValSerGlnArg
ENST00000350026.10:c.4497_4498insTCTTCTCACGTCAGCCAGCGG	ENSP00000055163.7:p.Trp1499_Pro1500insSerSerHisValSerGlnArg
ENST00000414678.7:c.3063_3064insTCTTCTCACGTCAGCCAGCGG	ENSP00000412835.2:p.Trp1021_Pro1022insSerSerHisValSerGlnArg
ENST00000635849.1:c.2226_2227insTCTTCTCACGTCAGCCAGCGG	ENSP00000490948.1:p.Trp742_Pro743insSerSerHisValSerGlnArg
ENST00000635957.1:c.1857_1858insTCTTCTCACGTCAGCCAGCGG	ENSP00000490385.1:p.Trp619_Pro620insSerSerHisValSerGlnArg
ENST00000636227.1:n.3368_3369insTCTTCTCACGTCAGCCAGCGG
ENST00000636254.1:n.825_826insTCTTCTCACGTCAGCCAGCGG
ENST00000636930.2:c.4905_4906insTCTTCTCACGTCAGCCAGCGG MANE Select	ENSP00000490491.2:p.Trp1635_Pro1636insSerSerHisValSerGlnArg
ENST00000636940.1:n.2902_2903insTCTTCTCACGTCAGCCAGCGG
ENST00000637015.1:c.2273_2274insTCTTCTCACGTCAGCCAGCGG
ENST00000637568.1:c.2187_2188insTCTTCTCACGTCAGCCAGCGG
ENST00000637741.1:n.1571_1572insTCTTCTCACGTCAGCCAGCGG
ENST00000637810.1:c.2247_2248insTCTTCTCACGTCAGCCAGCGG	ENSP00000489636.1:p.Trp749_Pro750insSerSerHisValSerGlnArg
ENST00000637904.1:c.2406_2407insTCTTCTCACGTCAGCCAGCGG	ENSP00000490550.1:p.Trp802_Pro803insSerSerHisValSerGlnArg
ENST00000647938.1:c.4536_4537insTCTTCTCACGTCAGCCAGCGG	ENSP00000498155.1:p.Trp1512_Pro1513insSerSerHisValSerGlnArg
ENST00000346085.9:c.4536_4537insTCTTCTCACGTCAGCCAGCGG	ENSP00000344546.4:p.Trp1512_Pro1513insSerSerHisValSerGlnArg
ENST00000350026.9:c.4497_4498insTCTTCTCACGTCAGCCAGCGG	ENSP00000055163.7:p.Trp1499_Pro1500insSerSerHisValSerGlnArg
ENST00000414678.6:c.3063_3064insTCTTCTCACGTCAGCCAGCGG	ENSP00000412835.2:p.Trp1021_Pro1022insSerSerHisValSerGlnArg
NM_017519.2:c.4497_4498insTCTTCTCACGTCAGCCAGCGG	NP_059989.2:p.Trp1499_Pro1500insSerSerHisValSerGlnArg
NM_020732.3:c.4536_4537insTCTTCTCACGTCAGCCAGCGG	NP_065783.3:p.Trp1512_Pro1513insSerSerHisValSerGlnArg
XM_005267069.3:c.4656_4657insTCTTCTCACGTCAGCCAGCGG	XP_005267126.2:p.Trp1552_Pro1553insSerSerHisValSerGlnArg
XM_011535984.1:c.3735_3736insTCTTCTCACGTCAGCCAGCGG	XP_011534286.1:p.Trp1245_Pro1246insSerSerHisValSerGlnArg
XM_011535985.1:c.3555_3556insTCTTCTCACGTCAGCCAGCGG	XP_011534287.1:p.Trp1185_Pro1186insSerSerHisValSerGlnArg
XM_011535986.1:c.3315_3316insTCTTCTCACGTCAGCCAGCGG	XP_011534288.1:p.Trp1105_Pro1106insSerSerHisValSerGlnArg
XM_011535987.1:c.2934_2935insTCTTCTCACGTCAGCCAGCGG	XP_011534289.1:p.Trp978_Pro979insSerSerHisValSerGlnArg
XM_011535988.1:c.1797_1798insTCTTCTCACGTCAGCCAGCGG	XP_011534290.1:p.Trp599_Pro600insSerSerHisValSerGlnArg
NM_001346813.1:c.4656_4657insTCTTCTCACGTCAGCCAGCGG	NP_001333742.1:p.Trp1552_Pro1553insSerSerHisValSerGlnArg
NM_001363725.1:c.2406_2407insTCTTCTCACGTCAGCCAGCGG	NP_001350654.1:p.Trp802_Pro803insSerSerHisValSerGlnArg
XM_011535984.2:c.4866_4867insTCTTCTCACGTCAGCCAGCGG	XP_011534286.2:p.Trp1622_Pro1623insSerSerHisValSerGlnArg
XM_011535988.3:c.1797_1798insTCTTCTCACGTCAGCCAGCGG	XP_011534290.1:p.Trp599_Pro600insSerSerHisValSerGlnArg
XM_017011103.2:c.4767_4768insTCTTCTCACGTCAGCCAGCGG	XP_016866592.1:p.Trp1589_Pro1590insSerSerHisValSerGlnArg
XM_017011104.1:c.4737_4738insTCTTCTCACGTCAGCCAGCGG	XP_016866593.1:p.Trp1579_Pro1580insSerSerHisValSerGlnArg
XM_017011105.2:c.4707_4708insTCTTCTCACGTCAGCCAGCGG	XP_016866594.1:p.Trp1569_Pro1570insSerSerHisValSerGlnArg
XM_017011106.2:c.4578_4579insTCTTCTCACGTCAGCCAGCGG	XP_016866595.1:p.Trp1526_Pro1527insSerSerHisValSerGlnArg
XM_017011107.2:c.4557_4558insTCTTCTCACGTCAGCCAGCGG	XP_016866596.1:p.Trp1519_Pro1520insSerSerHisValSerGlnArg
XR_002956289.1:n.4852_4853insTCTTCTCACGTCAGCCAGCGG
NM_001363725.2:c.2406_2407insTCTTCTCACGTCAGCCAGCGG	NP_001350654.1:p.Trp802_Pro803insSerSerHisValSerGlnArg
NM_001371656.1:c.4785_4786insTCTTCTCACGTCAGCCAGCGG	NP_001358585.1:p.Trp1595_Pro1596insSerSerHisValSerGlnArg
NM_001374820.1:c.4785_4786insTCTTCTCACGTCAGCCAGCGG	NP_001361749.1:p.Trp1595_Pro1596insSerSerHisValSerGlnArg
NM_001374828.1:c.4905_4906insTCTTCTCACGTCAGCCAGCGG MANE Select	NP_001361757.1:p.Trp1635_Pro1636insSerSerHisValSerGlnArg
NM_017519.3:c.4746_4747insTCTTCTCACGTCAGCCAGCGG	NP_059989.3:p.Trp1582_Pro1583insSerSerHisValSerGlnArg