Canonical Allele Identifier: CA915944793

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 666286
• ClinVar RCV Id: RCV000824815
• dbSNP Id: rs1583280025

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084793_157084812del , CM000668.2:g.157084793_157084812del	GRCh38
NC_000006.11:g.157405927_157405946del , CM000668.1:g.157405927_157405946del	GRCh37
NC_000006.10:g.157447619_157447638del	NCBI36
NG_032093.1:g.311864_311883del
NG_032093.2:g.311864_311883del
NG_066624.1:g.313768_313787del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2379_2398del	ENSP00000055163.8:p.His793GlnfsTer?
ENST00000414678.8:c.2379_2398del	ENSP00000412835.3:p.His793GlnfsTer?
ENST00000637015.2:c.2379_2398del	ENSP00000489729.2:p.His793GlnfsTer?
ENST00000319584.11:c.393_412del	ENSP00000313006.7:p.His131GlnfsTer?
ENST00000346085.10:c.2418_2437del	ENSP00000344546.5:p.His806GlnfsTer?
ENST00000350026.10:c.2130_2149del	ENSP00000055163.7:p.His710GlnfsTer?
ENST00000414678.7:c.627_646del	ENSP00000412835.2:p.His209GlnfsTer?
ENST00000452544.2:n.280_299del
ENST00000493658.2:n.28_47del
ENST00000635849.1:c.-121_-102del	ENSP00000490948.1:n.-121_-102del
ENST00000636930.2:c.2379_2398del MANE Select	ENSP00000490491.2:p.His793GlnfsTer?
ENST00000637003.1:c.-121_-102del	ENSP00000489666.1:n.-121_-102del
ENST00000637810.1:c.-121_-102del	ENSP00000489636.1:n.-121_-102del
ENST00000637904.1:c.-121_-102del	ENSP00000490550.1:n.-121_-102del
ENST00000647938.1:c.2169_2188del	ENSP00000498155.1:p.His723GlnfsTer?
ENST00000674190.1:n.1128_1147del
ENST00000319584.10:c.396_415del	ENSP00000313006.6:p.His132GlnfsTer?
ENST00000346085.9:c.2169_2188del	ENSP00000344546.4:p.His723GlnfsTer?
ENST00000350026.9:c.2130_2149del	ENSP00000055163.7:p.His710GlnfsTer?
ENST00000414678.6:c.627_646del	ENSP00000412835.2:p.His209GlnfsTer?
ENST00000452544.1:n.238_257del
ENST00000493658.1:n.28_47del
NM_017519.2:c.2130_2149del	NP_059989.2:p.His710GlnfsTer?
NM_020732.3:c.2169_2188del	NP_065783.3:p.His723GlnfsTer?
XM_005267069.3:c.2130_2149del	XP_005267126.2:p.His710GlnfsTer?
XM_011535984.1:c.1080_1099del	XP_011534286.1:p.His360GlnfsTer?
XM_011535985.1:c.1080_1099del	XP_011534287.1:p.His360GlnfsTer?
XM_011535986.1:c.660_679del	XP_011534288.1:p.His220GlnfsTer?
XM_011535987.1:c.279_298del	XP_011534289.1:p.His93GlnfsTer?
NM_001346813.1:c.2130_2149del	NP_001333742.1:p.His710GlnfsTer?
NM_001363725.1:c.-121_-102del	NP_001350654.1:n.-121_-102del
XM_011535984.2:c.2211_2230del	XP_011534286.2:p.His737GlnfsTer?
XM_017011103.2:c.2211_2230del	XP_016866592.1:p.His737GlnfsTer?
XM_017011104.1:c.2211_2230del	XP_016866593.1:p.His737GlnfsTer?
XM_017011105.2:c.2211_2230del	XP_016866594.1:p.His737GlnfsTer?
XM_017011106.2:c.2211_2230del	XP_016866595.1:p.His737GlnfsTer?
XM_017011107.2:c.2211_2230del	XP_016866596.1:p.His737GlnfsTer?
XR_002956289.1:n.2294_2313del
NM_001363725.2:c.-121_-102del	NP_001350654.1:n.-121_-102del
NM_001371656.1:c.2418_2437del	NP_001358585.1:p.His806GlnfsTer?
NM_001374820.1:c.2418_2437del	NP_001361749.1:p.His806GlnfsTer?
NM_001374828.1:c.2379_2398del MANE Select	NP_001361757.1:p.His793GlnfsTer?
NM_017519.3:c.2379_2398del	NP_059989.3:p.His793GlnfsTer?