Canonical Allele Identifier: CA913109713

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522190del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201060del , CM000668.2:g.157201060del	GRCh38
NC_000006.11:g.157522194del , CM000668.1:g.157522194del	GRCh37
NC_000006.10:g.157563886del	NCBI36
NG_032093.1:g.428131del
NG_032093.2:g.428131del
NG_066624.1:g.430035del

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4676del	ENSP00000055163.8:p.Pro1559LeufsTer5
ENST00000414678.8:c.4745del	ENSP00000412835.3:p.Pro1582LeufsTer5
ENST00000637015.2:c.4964del	ENSP00000489729.2:p.Pro1655LeufsTer5
ENST00000346085.10:c.4715del	ENSP00000344546.5:p.Pro1572LeufsTer5
ENST00000350026.10:c.4427del	ENSP00000055163.7:p.Pro1476LeufsTer5
ENST00000414678.7:c.2993del	ENSP00000412835.2:p.Pro998LeufsTer5
ENST00000635849.1:c.2156del	ENSP00000490948.1:p.Pro719LeufsTer5
ENST00000635957.1:c.1787del	ENSP00000490385.1:p.Pro596LeufsTer5
ENST00000636227.1:n.3298del
ENST00000636254.1:n.755del
ENST00000636930.2:c.4835del MANE Select	ENSP00000490491.2:p.Pro1612LeufsTer5
ENST00000636940.1:n.2832del
ENST00000637015.1:c.2203del
ENST00000637568.1:c.2117del
ENST00000637741.1:n.1501del
ENST00000637810.1:c.2177del	ENSP00000489636.1:p.Pro726LeufsTer5
ENST00000637904.1:c.2336del	ENSP00000490550.1:p.Pro779LeufsTer5
ENST00000647938.1:c.4466del	ENSP00000498155.1:p.Pro1489LeufsTer5
ENST00000346085.9:c.4466del	ENSP00000344546.4:p.Pro1489LeufsTer5
ENST00000350026.9:c.4427del	ENSP00000055163.7:p.Pro1476LeufsTer5
ENST00000414678.6:c.2993del	ENSP00000412835.2:p.Pro998LeufsTer5
NM_017519.2:c.4427del	NP_059989.2:p.Pro1476LeufsTer5
NM_020732.3:c.4466del	NP_065783.3:p.Pro1489LeufsTer5
XM_005267069.3:c.4586del	XP_005267126.2:p.Pro1529LeufsTer5
XM_011535984.1:c.3665del	XP_011534286.1:p.Pro1222LeufsTer5
XM_011535985.1:c.3485del	XP_011534287.1:p.Pro1162LeufsTer5
XM_011535986.1:c.3245del	XP_011534288.1:p.Pro1082LeufsTer5
XM_011535987.1:c.2864del	XP_011534289.1:p.Pro955LeufsTer5
XM_011535988.1:c.1727del	XP_011534290.1:p.Pro576LeufsTer5
NM_001346813.1:c.4586del	NP_001333742.1:p.Pro1529LeufsTer5
NM_001363725.1:c.2336del	NP_001350654.1:p.Pro779LeufsTer5
XM_011535984.2:c.4796del	XP_011534286.2:p.Pro1599LeufsTer5
XM_011535988.3:c.1727del	XP_011534290.1:p.Pro576LeufsTer5
XM_017011103.2:c.4697del	XP_016866592.1:p.Pro1566LeufsTer5
XM_017011104.1:c.4667del	XP_016866593.1:p.Pro1556LeufsTer5
XM_017011105.2:c.4637del	XP_016866594.1:p.Pro1546LeufsTer5
XM_017011106.2:c.4508del	XP_016866595.1:p.Pro1503LeufsTer5
XM_017011107.2:c.4487del	XP_016866596.1:p.Pro1496LeufsTer5
XR_002956289.1:n.4782del
NM_001363725.2:c.2336del	NP_001350654.1:p.Pro779LeufsTer5
NM_001371656.1:c.4715del	NP_001358585.1:p.Pro1572LeufsTer5
NM_001374820.1:c.4715del	NP_001361749.1:p.Pro1572LeufsTer5
NM_001374828.1:c.4835del MANE Select	NP_001361757.1:p.Pro1612LeufsTer5
NM_017519.3:c.4676del	NP_059989.3:p.Pro1559LeufsTer5