Canonical Allele Identifier: CA2695207242

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181033del , CM000668.2:g.157181033del	GRCh38
NC_000006.11:g.157502167del , CM000668.1:g.157502167del	GRCh37
NC_000006.10:g.157543859del	NCBI36
NG_032093.1:g.408104del
NG_032093.2:g.408104del
NG_066624.1:g.410008del

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3410del	ENSP00000055163.8:p.Pro1137GlnfsTer?
ENST00000414678.8:c.3479del	ENSP00000412835.3:p.Pro1160GlnfsTer?
ENST00000637015.2:c.3698del	ENSP00000489729.2:p.Pro1233GlnfsTer?
ENST00000319584.11:c.1583del	ENSP00000313006.7:p.Pro528GlnfsTer?
ENST00000346085.10:c.3449del	ENSP00000344546.5:p.Pro1150GlnfsTer?
ENST00000350026.10:c.3161del	ENSP00000055163.7:p.Pro1054GlnfsTer?
ENST00000414678.7:c.1727del	ENSP00000412835.2:p.Pro576GlnfsTer?
ENST00000635849.1:c.890del	ENSP00000490948.1:p.Pro297GlnfsTer?
ENST00000635957.1:c.524del	ENSP00000490385.1:p.Pro175GlnfsTer?
ENST00000636930.2:c.3569del MANE Select	ENSP00000490491.2:p.Pro1190GlnfsTer?
ENST00000636940.1:n.1566del
ENST00000637015.1:c.937del
ENST00000637568.1:c.851del
ENST00000637741.1:n.235del
ENST00000637810.1:c.911del	ENSP00000489636.1:p.Pro304GlnfsTer?
ENST00000637904.1:c.1070del	ENSP00000490550.1:p.Pro357GlnfsTer?
ENST00000647938.1:c.3200del	ENSP00000498155.1:p.Pro1067GlnfsTer?
ENST00000319584.10:c.1586del	ENSP00000313006.6:p.Pro529GlnfsTer?
ENST00000346085.9:c.3200del	ENSP00000344546.4:p.Pro1067GlnfsTer?
ENST00000350026.9:c.3161del	ENSP00000055163.7:p.Pro1054GlnfsTer?
ENST00000400790.3:c.362del	ENSP00000383596.3:p.Pro121GlnfsTer?
ENST00000414678.6:c.1727del	ENSP00000412835.2:p.Pro576GlnfsTer?
ENST00000478761.3:c.771del
NM_017519.2:c.3161del	NP_059989.2:p.Pro1054GlnfsTer?
NM_020732.3:c.3200del	NP_065783.3:p.Pro1067GlnfsTer?
XM_005267069.3:c.3320del	XP_005267126.2:p.Pro1107GlnfsTer?
XM_011535984.1:c.2399del	XP_011534286.1:p.Pro800GlnfsTer?
XM_011535985.1:c.2219del	XP_011534287.1:p.Pro740GlnfsTer?
XM_011535986.1:c.1979del	XP_011534288.1:p.Pro660GlnfsTer?
XM_011535987.1:c.1598del	XP_011534289.1:p.Pro533GlnfsTer?
XM_011535988.1:c.461del	XP_011534290.1:p.Pro154GlnfsTer?
NM_001346813.1:c.3320del	NP_001333742.1:p.Pro1107GlnfsTer?
NM_001363725.1:c.1070del	NP_001350654.1:p.Pro357GlnfsTer?
XM_011535984.2:c.3530del	XP_011534286.2:p.Pro1177GlnfsTer?
XM_011535988.3:c.461del	XP_011534290.1:p.Pro154GlnfsTer?
XM_017011103.2:c.3431del	XP_016866592.1:p.Pro1144GlnfsTer?
XM_017011104.1:c.3401del	XP_016866593.1:p.Pro1134GlnfsTer?
XM_017011105.2:c.3371del	XP_016866594.1:p.Pro1124GlnfsTer?
XM_017011106.2:c.3242del	XP_016866595.1:p.Pro1081GlnfsTer?
XM_017011107.2:c.3221del	XP_016866596.1:p.Pro1074GlnfsTer?
XR_002956289.1:n.3613del
NM_001363725.2:c.1070del	NP_001350654.1:p.Pro357GlnfsTer?
NM_001371656.1:c.3449del	NP_001358585.1:p.Pro1150GlnfsTer?
NM_001374820.1:c.3449del	NP_001361749.1:p.Pro1150GlnfsTer?
NM_001374828.1:c.3569del MANE Select	NP_001361757.1:p.Pro1190GlnfsTer?
NM_017519.3:c.3410del	NP_059989.3:p.Pro1137GlnfsTer?