Canonical Allele Identifier: CA1675400830

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901543_156901551delinsCCCCGCAGG , CM000668.2:g.156901543_156901551delinsCCCCGCAGG	GRCh38
NC_000006.11:g.157222677_157222685delinsCCCCGCAGG , CM000668.1:g.157222677_157222685delinsCCCCGCAGG	GRCh37
NC_000006.10:g.157264369_157264377delinsCCCCGCAGG	NCBI36
NG_032093.1:g.128614_128622delinsCCCCGCAGG
NG_032093.2:g.128614_128622delinsCCCCGCAGG
NG_066624.1:g.130518_130526delinsCCCCGCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2136+18_2136+26delinsCCCCGCAGG	ENSP00000055163.8:n.2136+18_2136+26delinsCCCCGCAGG
ENST00000414678.8:c.2136+18_2136+26delinsCCCCGCAGG	ENSP00000412835.3:n.2136+18_2136+26delinsCCCCGCAGG
ENST00000637015.2:c.2136+18_2136+26delinsCCCCGCAGG	ENSP00000489729.2:n.2136+18_2136+26delinsCCCCGCAGG
ENST00000319584.11:c.150+18_150+26delinsCCCCGCAGG	ENSP00000313006.7:n.150+18_150+26delinsCCCCGCAGG
ENST00000346085.10:c.2175+18_2175+26delinsCCCCGCAGG	ENSP00000344546.5:n.2175+18_2175+26delinsCCCCGCAGG
ENST00000350026.10:c.1887+18_1887+26delinsCCCCGCAGG	ENSP00000055163.7:n.1887+18_1887+26delinsCCCCGCAGG
ENST00000414678.7:c.384+18_384+26delinsCCCCGCAGG	ENSP00000412835.2:n.384+18_384+26delinsCCCCGCAGG
ENST00000636205.1:n.217_225delinsCCCCGCAGG
ENST00000636748.1:c.417+18_417+26delinsCCCCGCAGG	ENSP00000489917.1:n.417+18_417+26delinsCCCCGCAGG
ENST00000636930.2:c.2136+18_2136+26delinsCCCCGCAGG MANE Select	ENSP00000490491.2:n.2136+18_2136+26delinsCCCCGCAGG
ENST00000637532.1:c.162+18_162+26delinsCCCCGCAGG	ENSP00000490420.1:n.162+18_162+26delinsCCCCGCAGG
ENST00000638000.1:c.353+18_353+26delinsCCCCGCAGG
ENST00000647938.1:c.1926+18_1926+26delinsCCCCGCAGG	ENSP00000498155.1:n.1926+18_1926+26delinsCCCCGCAGG
ENST00000674190.1:n.843+18_843+26delinsCCCCGCAGG
ENST00000674298.1:c.1876+18_1876+26delinsCCCCGCAGG
ENST00000319584.10:c.153+18_153+26delinsCCCCGCAGG	ENSP00000313006.6:n.153+18_153+26delinsCCCCGCAGG
ENST00000346085.9:c.1926+18_1926+26delinsCCCCGCAGG	ENSP00000344546.4:n.1926+18_1926+26delinsCCCCGCAGG
ENST00000350026.9:c.1887+18_1887+26delinsCCCCGCAGG	ENSP00000055163.7:n.1887+18_1887+26delinsCCCCGCAGG
ENST00000414678.6:c.384+18_384+26delinsCCCCGCAGG	ENSP00000412835.2:n.384+18_384+26delinsCCCCGCAGG
NM_017519.2:c.1887+18_1887+26delinsCCCCGCAGG	NP_059989.2:n.1887+18_1887+26delinsCCCCGCAGG
NM_020732.3:c.1926+18_1926+26delinsCCCCGCAGG	NP_065783.3:n.1926+18_1926+26delinsCCCCGCAGG
XM_005267069.3:c.1887+18_1887+26delinsCCCCGCAGG	XP_005267126.2:n.1887+18_1887+26delinsCCCCGCAGG
XM_011535984.1:c.795+18_795+26delinsCCCCGCAGG	XP_011534286.1:n.795+18_795+26delinsCCCCGCAGG
XM_011535985.1:c.795+18_795+26delinsCCCCGCAGG	XP_011534287.1:n.795+18_795+26delinsCCCCGCAGG
XM_011535986.1:c.375+18_375+26delinsCCCCGCAGG	XP_011534288.1:n.375+18_375+26delinsCCCCGCAGG
NM_001346813.1:c.1887+18_1887+26delinsCCCCGCAGG	NP_001333742.1:n.1887+18_1887+26delinsCCCCGCAGG
XM_011535984.2:c.1926+18_1926+26delinsCCCCGCAGG	XP_011534286.2:n.1926+18_1926+26delinsCCCCGCAGG
XM_017011103.2:c.1926+18_1926+26delinsCCCCGCAGG	XP_016866592.1:n.1926+18_1926+26delinsCCCCGCAGG
XM_017011104.1:c.1926+18_1926+26delinsCCCCGCAGG	XP_016866593.1:n.1926+18_1926+26delinsCCCCGCAGG
XM_017011105.2:c.1926+18_1926+26delinsCCCCGCAGG	XP_016866594.1:n.1926+18_1926+26delinsCCCCGCAGG
XM_017011106.2:c.1926+18_1926+26delinsCCCCGCAGG	XP_016866595.1:n.1926+18_1926+26delinsCCCCGCAGG
XM_017011107.2:c.1926+18_1926+26delinsCCCCGCAGG	XP_016866596.1:n.1926+18_1926+26delinsCCCCGCAGG
XR_002956289.1:n.2009+18_2009+26delinsCCCCGCAGG
NM_001371656.1:c.2175+18_2175+26delinsCCCCGCAGG	NP_001358585.1:n.2175+18_2175+26delinsCCCCGCAGG
NM_001374820.1:c.2175+18_2175+26delinsCCCCGCAGG	NP_001361749.1:n.2175+18_2175+26delinsCCCCGCAGG
NM_001374828.1:c.2136+18_2136+26delinsCCCCGCAGG MANE Select	NP_001361757.1:n.2136+18_2136+26delinsCCCCGCAGG
NM_017519.3:c.2136+18_2136+26delinsCCCCGCAGG	NP_059989.3:n.2136+18_2136+26delinsCCCCGCAGG