Canonical Allele Identifier: CA2695207243

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181069del , CM000668.2:g.157181069del	GRCh38
NC_000006.11:g.157502203del , CM000668.1:g.157502203del	GRCh37
NC_000006.10:g.157543895del	NCBI36
NG_032093.1:g.408140del
NG_032093.2:g.408140del
NG_066624.1:g.410044del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3446del	ENSP00000055163.8:p.Phe1149SerfsTer?
ENST00000414678.8:c.3515del	ENSP00000412835.3:p.Phe1172SerfsTer?
ENST00000637015.2:c.3734del	ENSP00000489729.2:p.Phe1245SerfsTer?
ENST00000319584.11:c.1619del	ENSP00000313006.7:p.Phe540SerfsTer?
ENST00000346085.10:c.3485del	ENSP00000344546.5:p.Phe1162SerfsTer?
ENST00000350026.10:c.3197del	ENSP00000055163.7:p.Phe1066SerfsTer?
ENST00000414678.7:c.1763del	ENSP00000412835.2:p.Phe588SerfsTer?
ENST00000635849.1:c.926del	ENSP00000490948.1:p.Phe309SerfsTer?
ENST00000635957.1:c.560del	ENSP00000490385.1:p.Phe187SerfsTer?
ENST00000636930.2:c.3605del MANE Select	ENSP00000490491.2:p.Phe1202SerfsTer?
ENST00000636940.1:n.1602del
ENST00000637015.1:c.973del
ENST00000637568.1:c.887del
ENST00000637741.1:n.271del
ENST00000637810.1:c.947del	ENSP00000489636.1:p.Phe316SerfsTer?
ENST00000637904.1:c.1106del	ENSP00000490550.1:p.Phe369SerfsTer?
ENST00000647938.1:c.3236del	ENSP00000498155.1:p.Phe1079SerfsTer?
ENST00000319584.10:c.1622del	ENSP00000313006.6:p.Phe541SerfsTer?
ENST00000346085.9:c.3236del	ENSP00000344546.4:p.Phe1079SerfsTer?
ENST00000350026.9:c.3197del	ENSP00000055163.7:p.Phe1066SerfsTer?
ENST00000400790.3:c.398del	ENSP00000383596.3:p.Phe133SerfsTer?
ENST00000414678.6:c.1763del	ENSP00000412835.2:p.Phe588SerfsTer?
ENST00000478761.3:c.807del
NM_017519.2:c.3197del	NP_059989.2:p.Phe1066SerfsTer?
NM_020732.3:c.3236del	NP_065783.3:p.Phe1079SerfsTer?
XM_005267069.3:c.3356del	XP_005267126.2:p.Phe1119SerfsTer?
XM_011535984.1:c.2435del	XP_011534286.1:p.Phe812SerfsTer?
XM_011535985.1:c.2255del	XP_011534287.1:p.Phe752SerfsTer?
XM_011535986.1:c.2015del	XP_011534288.1:p.Phe672SerfsTer?
XM_011535987.1:c.1634del	XP_011534289.1:p.Phe545SerfsTer?
XM_011535988.1:c.497del	XP_011534290.1:p.Phe166SerfsTer?
NM_001346813.1:c.3356del	NP_001333742.1:p.Phe1119SerfsTer?
NM_001363725.1:c.1106del	NP_001350654.1:p.Phe369SerfsTer?
XM_011535984.2:c.3566del	XP_011534286.2:p.Phe1189SerfsTer?
XM_011535988.3:c.497del	XP_011534290.1:p.Phe166SerfsTer?
XM_017011103.2:c.3467del	XP_016866592.1:p.Phe1156SerfsTer?
XM_017011104.1:c.3437del	XP_016866593.1:p.Phe1146SerfsTer?
XM_017011105.2:c.3407del	XP_016866594.1:p.Phe1136SerfsTer?
XM_017011106.2:c.3278del	XP_016866595.1:p.Phe1093SerfsTer?
XM_017011107.2:c.3257del	XP_016866596.1:p.Phe1086SerfsTer?
XR_002956289.1:n.3649del
NM_001363725.2:c.1106del	NP_001350654.1:p.Phe369SerfsTer?
NM_001371656.1:c.3485del	NP_001358585.1:p.Phe1162SerfsTer?
NM_001374820.1:c.3485del	NP_001361749.1:p.Phe1162SerfsTer?
NM_001374828.1:c.3605del MANE Select	NP_001361757.1:p.Phe1202SerfsTer?
NM_017519.3:c.3446del	NP_059989.3:p.Phe1149SerfsTer?