Canonical Allele Identifier: CA2695207306

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148949del , CM000668.2:g.157148949del	GRCh38
NC_000006.11:g.157470083del , CM000668.1:g.157470083del	GRCh37
NC_000006.10:g.157511775del	NCBI36
NG_032093.1:g.376020del
NG_032093.2:g.376020del
NG_066624.1:g.377924del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3087del	ENSP00000055163.8:p.Ser1029ArgfsTer9
ENST00000414678.8:c.2997del	ENSP00000412835.3:p.Ser999ArgfsTer9
ENST00000637015.2:c.3087del	ENSP00000489729.2:p.Ser1029ArgfsTer?
ENST00000319584.11:c.1101del	ENSP00000313006.7:p.Ser367ArgfsTer9
ENST00000346085.10:c.3126del	ENSP00000344546.5:p.Ser1042ArgfsTer9
ENST00000350026.10:c.2838del	ENSP00000055163.7:p.Ser946ArgfsTer9
ENST00000414678.7:c.1245del	ENSP00000412835.2:p.Ser415ArgfsTer9
ENST00000452544.2:n.988del
ENST00000635849.1:c.408del	ENSP00000490948.1:p.Ser136ArgfsTer9
ENST00000635957.1:c.42del	ENSP00000490385.1:p.Ser14ArgfsTer9
ENST00000636426.1:n.221del
ENST00000636930.2:c.3087del MANE Select	ENSP00000490491.2:p.Ser1029ArgfsTer9
ENST00000637015.1:c.326del
ENST00000637568.1:c.130del
ENST00000637810.1:c.588del	ENSP00000489636.1:p.Ser196ArgfsTer9
ENST00000637904.1:c.588del	ENSP00000490550.1:p.Ser196ArgfsTer9
ENST00000647938.1:c.2877del	ENSP00000498155.1:p.Ser959ArgfsTer9
ENST00000674190.1:n.1836del
ENST00000319584.10:c.1104del	ENSP00000313006.6:p.Ser368ArgfsTer9
ENST00000346085.9:c.2877del	ENSP00000344546.4:p.Ser959ArgfsTer9
ENST00000350026.9:c.2838del	ENSP00000055163.7:p.Ser946ArgfsTer9
ENST00000400790.3:c.39del	ENSP00000383596.3:p.Ser13ArgfsTer9
ENST00000414678.6:c.1245del	ENSP00000412835.2:p.Ser415ArgfsTer9
ENST00000452544.1:n.934del
ENST00000478761.3:c.160del
NM_017519.2:c.2838del	NP_059989.2:p.Ser946ArgfsTer9
NM_020732.3:c.2877del	NP_065783.3:p.Ser959ArgfsTer9
XM_005267069.3:c.2838del	XP_005267126.2:p.Ser946ArgfsTer9
XM_011535984.1:c.1788del	XP_011534286.1:p.Ser596ArgfsTer?
XM_011535985.1:c.1608del	XP_011534287.1:p.Ser536ArgfsTer?
XM_011535986.1:c.1368del	XP_011534288.1:p.Ser456ArgfsTer?
XM_011535987.1:c.987del	XP_011534289.1:p.Ser329ArgfsTer?
XM_011535988.1:c.-20+15742del	XP_011534290.1:n.-20+15742del
NM_001346813.1:c.2838del	NP_001333742.1:p.Ser946ArgfsTer9
NM_001363725.1:c.588del	NP_001350654.1:p.Ser196ArgfsTer9
XM_011535984.2:c.2919del	XP_011534286.2:p.Ser973ArgfsTer?
XM_011535988.3:c.-20+15742del	XP_011534290.1:n.-20+15742del
XM_017011103.2:c.2919del	XP_016866592.1:p.Ser973ArgfsTer19
XM_017011104.1:c.2919del	XP_016866593.1:p.Ser973ArgfsTer9
XM_017011105.2:c.2919del	XP_016866594.1:p.Ser973ArgfsTer?
XM_017011106.2:c.2919del	XP_016866595.1:p.Ser973ArgfsTer9
XM_017011107.2:c.2739del	XP_016866596.1:p.Ser913ArgfsTer9
XR_002956289.1:n.3002del
NM_001363725.2:c.588del	NP_001350654.1:p.Ser196ArgfsTer9
NM_001371656.1:c.3126del	NP_001358585.1:p.Ser1042ArgfsTer9
NM_001374820.1:c.3126del	NP_001361749.1:p.Ser1042ArgfsTer9
NM_001374828.1:c.3087del MANE Select	NP_001361757.1:p.Ser1029ArgfsTer9
NM_017519.3:c.3087del	NP_059989.3:p.Ser1029ArgfsTer9