Canonical Allele Identifier: CA2695207222

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156829362_156829372del , CM000668.2:g.156829362_156829372del	GRCh38
NC_000006.11:g.157150496_157150506del , CM000668.1:g.157150496_157150506del	GRCh37
NC_000006.10:g.157192188_157192198del	NCBI36
NG_032093.1:g.56433_56443del
NG_032093.2:g.56433_56443del
NG_066624.1:g.58337_58347del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.1927_1937del	ENSP00000055163.8:p.Ile643GlyfsTer?
ENST00000414678.8:c.1927_1937del	ENSP00000412835.3:p.Ile643GlyfsTer?
ENST00000637015.2:c.1927_1937del	ENSP00000489729.2:p.Ile643GlyfsTer?
ENST00000346085.10:c.1927_1937del	ENSP00000344546.5:p.Ile643GlyfsTer?
ENST00000350026.10:c.1678_1688del	ENSP00000055163.7:p.Ile560GlyfsTer?
ENST00000414678.7:c.175_185del	ENSP00000412835.2:p.Ile59GlyfsTer?
ENST00000494260.2:c.208_218del	ENSP00000490094.1:p.Ile70GlyfsTer?
ENST00000636607.1:c.190_200del	ENSP00000490050.1:p.Ile64GlyfsTer?
ENST00000636748.1:c.208_218del	ENSP00000489917.1:p.Ile70GlyfsTer?
ENST00000636930.2:c.1927_1937del MANE Select	ENSP00000490491.2:p.Ile643GlyfsTer?
ENST00000637910.1:n.208_218del
ENST00000638000.1:c.144_154del
ENST00000647938.1:c.1678_1688del	ENSP00000498155.1:p.Ile560GlyfsTer?
ENST00000674190.1:n.634_644del
ENST00000674298.1:c.1667_1677del
ENST00000346085.9:c.1678_1688del	ENSP00000344546.4:p.Ile560GlyfsTer?
ENST00000350026.9:c.1678_1688del	ENSP00000055163.7:p.Ile560GlyfsTer?
ENST00000414678.6:c.175_185del	ENSP00000412835.2:p.Ile59GlyfsTer?
ENST00000494260.1:n.136_146del
NM_017519.2:c.1678_1688del	NP_059989.2:p.Ile560GlyfsTer?
NM_020732.3:c.1678_1688del	NP_065783.3:p.Ile560GlyfsTer?
XM_005267069.3:c.1678_1688del	XP_005267126.2:p.Ile560GlyfsTer?
XM_011535984.1:c.547_557del	XP_011534286.1:p.Ile183GlyfsTer?
XM_011535985.1:c.547_557del	XP_011534287.1:p.Ile183GlyfsTer?
XM_011535986.1:c.127_137del	XP_011534288.1:p.Ile43GlyfsTer?
NM_001346813.1:c.1678_1688del	NP_001333742.1:p.Ile560GlyfsTer?
XM_011535984.2:c.1678_1688del	XP_011534286.2:p.Ile560GlyfsTer?
XM_017011103.2:c.1678_1688del	XP_016866592.1:p.Ile560GlyfsTer?
XM_017011104.1:c.1678_1688del	XP_016866593.1:p.Ile560GlyfsTer?
XM_017011105.2:c.1678_1688del	XP_016866594.1:p.Ile560GlyfsTer?
XM_017011106.2:c.1678_1688del	XP_016866595.1:p.Ile560GlyfsTer?
XM_017011107.2:c.1678_1688del	XP_016866596.1:p.Ile560GlyfsTer?
XR_002956289.1:n.1761_1771del
NM_001371656.1:c.1927_1937del	NP_001358585.1:p.Ile643GlyfsTer?
NM_001374820.1:c.1927_1937del	NP_001361749.1:p.Ile643GlyfsTer?
NM_001374828.1:c.1927_1937del MANE Select	NP_001361757.1:p.Ile643GlyfsTer?
NM_017519.3:c.1927_1937del	NP_059989.3:p.Ile643GlyfsTer?