Canonical Allele Identifier: CA658789861

Gene: ARID1B

Linked Data

• PubMed: PMID:28135719

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148918_157148925del , CM000668.2:g.157148918_157148925del	GRCh38
NC_000006.11:g.157470052_157470059del , CM000668.1:g.157470052_157470059del	GRCh37
NC_000006.10:g.157511744_157511751del	NCBI36
NG_032093.1:g.375989_375996del
NG_032093.2:g.375989_375996del
NG_066624.1:g.377893_377900del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3056_3063del	ENSP00000055163.8:p.Val1019GlyfsTer?
ENST00000414678.8:c.2966_2973del	ENSP00000412835.3:p.Val989GlyfsTer?
ENST00000637015.2:c.3056_3063del	ENSP00000489729.2:p.Val1019GlyfsTer14
ENST00000319584.11:c.1070_1077del	ENSP00000313006.7:p.Val357GlyfsTer?
ENST00000346085.10:c.3095_3102del	ENSP00000344546.5:p.Val1032GlyfsTer?
ENST00000350026.10:c.2807_2814del	ENSP00000055163.7:p.Val936GlyfsTer?
ENST00000414678.7:c.1214_1221del	ENSP00000412835.2:p.Val405GlyfsTer?
ENST00000452544.2:n.957_964del
ENST00000635849.1:c.377_384del	ENSP00000490948.1:p.Val126GlyfsTer?
ENST00000635957.1:c.11_18del	ENSP00000490385.1:p.Val4GlyfsTer?
ENST00000636426.1:n.190_197del
ENST00000636930.2:c.3056_3063del MANE Select	ENSP00000490491.2:p.Val1019GlyfsTer?
ENST00000637015.1:c.295_302del
ENST00000637568.1:c.99_106del
ENST00000637810.1:c.557_564del	ENSP00000489636.1:p.Val186GlyfsTer?
ENST00000637904.1:c.557_564del	ENSP00000490550.1:p.Val186GlyfsTer?
ENST00000647938.1:c.2846_2853del	ENSP00000498155.1:p.Val949GlyfsTer?
ENST00000674190.1:n.1805_1812del
ENST00000319584.10:c.1073_1080del	ENSP00000313006.6:p.Val358GlyfsTer?
ENST00000346085.9:c.2846_2853del	ENSP00000344546.4:p.Val949GlyfsTer?
ENST00000350026.9:c.2807_2814del	ENSP00000055163.7:p.Val936GlyfsTer?
ENST00000400790.3:c.8_15del	ENSP00000383596.3:p.Val3GlyfsTer?
ENST00000414678.6:c.1214_1221del	ENSP00000412835.2:p.Val405GlyfsTer?
ENST00000452544.1:n.903_910del
ENST00000478761.3:c.129_136del
NM_017519.2:c.2807_2814del	NP_059989.2:p.Val936GlyfsTer?
NM_020732.3:c.2846_2853del	NP_065783.3:p.Val949GlyfsTer?
XM_005267069.3:c.2807_2814del	XP_005267126.2:p.Val936GlyfsTer?
XM_011535984.1:c.1757_1764del	XP_011534286.1:p.Val586GlyfsTer14
XM_011535985.1:c.1577_1584del	XP_011534287.1:p.Val526GlyfsTer14
XM_011535986.1:c.1337_1344del	XP_011534288.1:p.Val446GlyfsTer14
XM_011535987.1:c.956_963del	XP_011534289.1:p.Val319GlyfsTer14
XM_011535988.1:c.-20+15711_-20+15718del	XP_011534290.1:n.-20+15711_-20+15718del
NM_001346813.1:c.2807_2814del	NP_001333742.1:p.Val936GlyfsTer?
NM_001363725.1:c.557_564del	NP_001350654.1:p.Val186GlyfsTer?
XM_011535984.2:c.2888_2895del	XP_011534286.2:p.Val963GlyfsTer14
XM_011535988.3:c.-20+15711_-20+15718del	XP_011534290.1:n.-20+15711_-20+15718del
XM_017011103.2:c.2888_2895del	XP_016866592.1:p.Val963GlyfsTer?
XM_017011104.1:c.2888_2895del	XP_016866593.1:p.Val963GlyfsTer?
XM_017011105.2:c.2888_2895del	XP_016866594.1:p.Val963GlyfsTer14
XM_017011106.2:c.2888_2895del	XP_016866595.1:p.Val963GlyfsTer?
XM_017011107.2:c.2708_2715del	XP_016866596.1:p.Val903GlyfsTer?
XR_002956289.1:n.2971_2978del
NM_001363725.2:c.557_564del	NP_001350654.1:p.Val186GlyfsTer?
NM_001371656.1:c.3095_3102del	NP_001358585.1:p.Val1032GlyfsTer?
NM_001374820.1:c.3095_3102del	NP_001361749.1:p.Val1032GlyfsTer?
NM_001374828.1:c.3056_3063del MANE Select	NP_001361757.1:p.Val1019GlyfsTer?
NM_017519.3:c.3056_3063del	NP_059989.3:p.Val1019GlyfsTer?