Canonical Allele Identifier: CA2680891490

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201354-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201358del , CM000668.2:g.157201358del	GRCh38
NC_000006.11:g.157522492del , CM000668.1:g.157522492del	GRCh37
NC_000006.10:g.157564184del	NCBI36
NG_032093.1:g.428429del
NG_032093.2:g.428429del
NG_066624.1:g.430333del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4974del	ENSP00000055163.8:p.Thr1659HisfsTer25
ENST00000414678.8:c.5043del	ENSP00000412835.3:p.Thr1682HisfsTer25
ENST00000637015.2:c.5262del	ENSP00000489729.2:p.Thr1755HisfsTer25
ENST00000346085.10:c.5013del	ENSP00000344546.5:p.Thr1672HisfsTer25
ENST00000350026.10:c.4725del	ENSP00000055163.7:p.Thr1576HisfsTer25
ENST00000414678.7:c.3291del	ENSP00000412835.2:p.Thr1098HisfsTer25
ENST00000635849.1:c.2454del	ENSP00000490948.1:p.Thr819HisfsTer25
ENST00000635957.1:c.2085del	ENSP00000490385.1:p.Thr696HisfsTer25
ENST00000636227.1:n.3596del
ENST00000636254.1:n.1053del
ENST00000636930.2:c.5133del MANE Select	ENSP00000490491.2:p.Thr1712HisfsTer25
ENST00000636940.1:n.3130del
ENST00000637015.1:c.2501del
ENST00000637568.1:c.2415del
ENST00000637741.1:n.1799del
ENST00000637810.1:c.2475del	ENSP00000489636.1:p.Thr826HisfsTer25
ENST00000637904.1:c.2634del	ENSP00000490550.1:p.Thr879HisfsTer25
ENST00000647938.1:c.4764del	ENSP00000498155.1:p.Thr1589HisfsTer25
ENST00000346085.9:c.4764del	ENSP00000344546.4:p.Thr1589HisfsTer25
ENST00000350026.9:c.4725del	ENSP00000055163.7:p.Thr1576HisfsTer25
ENST00000414678.6:c.3291del	ENSP00000412835.2:p.Thr1098HisfsTer25
NM_017519.2:c.4725del	NP_059989.2:p.Thr1576HisfsTer25
NM_020732.3:c.4764del	NP_065783.3:p.Thr1589HisfsTer25
XM_005267069.3:c.4884del	XP_005267126.2:p.Thr1629HisfsTer25
XM_011535984.1:c.3963del	XP_011534286.1:p.Thr1322HisfsTer25
XM_011535985.1:c.3783del	XP_011534287.1:p.Thr1262HisfsTer25
XM_011535986.1:c.3543del	XP_011534288.1:p.Thr1182HisfsTer25
XM_011535987.1:c.3162del	XP_011534289.1:p.Thr1055HisfsTer25
XM_011535988.1:c.2025del	XP_011534290.1:p.Thr676HisfsTer25
NM_001346813.1:c.4884del	NP_001333742.1:p.Thr1629HisfsTer25
NM_001363725.1:c.2634del	NP_001350654.1:p.Thr879HisfsTer25
XM_011535984.2:c.5094del	XP_011534286.2:p.Thr1699HisfsTer25
XM_011535988.3:c.2025del	XP_011534290.1:p.Thr676HisfsTer25
XM_017011103.2:c.4995del	XP_016866592.1:p.Thr1666HisfsTer25
XM_017011104.1:c.4965del	XP_016866593.1:p.Thr1656HisfsTer25
XM_017011105.2:c.4935del	XP_016866594.1:p.Thr1646HisfsTer25
XM_017011106.2:c.4806del	XP_016866595.1:p.Thr1603HisfsTer25
XM_017011107.2:c.4785del	XP_016866596.1:p.Thr1596HisfsTer25
XR_002956289.1:n.5080del
NM_001363725.2:c.2634del	NP_001350654.1:p.Thr879HisfsTer25
NM_001371656.1:c.5013del	NP_001358585.1:p.Thr1672HisfsTer25
NM_001374820.1:c.5013del	NP_001361749.1:p.Thr1672HisfsTer25
NM_001374828.1:c.5133del MANE Select	NP_001361757.1:p.Thr1712HisfsTer25
NM_017519.3:c.4974del	NP_059989.3:p.Thr1659HisfsTer25