Canonical Allele Identifier: CA658789860

Gene: ARID1B

Linked Data

• PubMed: PMID:28135719

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148868del , CM000668.2:g.157148868del	GRCh38
NC_000006.11:g.157470002del , CM000668.1:g.157470002del	GRCh37
NC_000006.10:g.157511694del	NCBI36
NG_032093.1:g.375939del
NG_032093.2:g.375939del
NG_066624.1:g.377843del

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3006del	ENSP00000055163.8:p.Pro1003ArgfsTer6
ENST00000414678.8:c.2916del	ENSP00000412835.3:p.Pro973ArgfsTer6
ENST00000637015.2:c.3006del	ENSP00000489729.2:p.Pro1003ArgfsTer6
ENST00000319584.11:c.1020del	ENSP00000313006.7:p.Pro341ArgfsTer6
ENST00000346085.10:c.3045del	ENSP00000344546.5:p.Pro1016ArgfsTer6
ENST00000350026.10:c.2757del	ENSP00000055163.7:p.Pro920ArgfsTer6
ENST00000414678.7:c.1164del	ENSP00000412835.2:p.Pro389ArgfsTer6
ENST00000452544.2:n.907del
ENST00000635849.1:c.327del	ENSP00000490948.1:p.Pro110ArgfsTer6
ENST00000636426.1:n.140del
ENST00000636930.2:c.3006del MANE Select	ENSP00000490491.2:p.Pro1003ArgfsTer6
ENST00000637015.1:c.245del
ENST00000637568.1:c.49del
ENST00000637810.1:c.507del	ENSP00000489636.1:p.Pro170ArgfsTer6
ENST00000637904.1:c.507del	ENSP00000490550.1:p.Pro170ArgfsTer6
ENST00000647938.1:c.2796del	ENSP00000498155.1:p.Pro933ArgfsTer6
ENST00000674190.1:n.1755del
ENST00000319584.10:c.1023del	ENSP00000313006.6:p.Pro342ArgfsTer6
ENST00000346085.9:c.2796del	ENSP00000344546.4:p.Pro933ArgfsTer6
ENST00000350026.9:c.2757del	ENSP00000055163.7:p.Pro920ArgfsTer6
ENST00000414678.6:c.1164del	ENSP00000412835.2:p.Pro389ArgfsTer6
ENST00000452544.1:n.853del
ENST00000478761.3:c.79del
NM_017519.2:c.2757del	NP_059989.2:p.Pro920ArgfsTer6
NM_020732.3:c.2796del	NP_065783.3:p.Pro933ArgfsTer6
XM_005267069.3:c.2757del	XP_005267126.2:p.Pro920ArgfsTer6
XM_011535984.1:c.1707del	XP_011534286.1:p.Pro570ArgfsTer6
XM_011535985.1:c.1527del	XP_011534287.1:p.Pro510ArgfsTer6
XM_011535986.1:c.1287del	XP_011534288.1:p.Pro430ArgfsTer6
XM_011535987.1:c.906del	XP_011534289.1:p.Pro303ArgfsTer6
XM_011535988.1:c.-20+15661del	XP_011534290.1:n.-20+15661del
NM_001346813.1:c.2757del	NP_001333742.1:p.Pro920ArgfsTer6
NM_001363725.1:c.507del	NP_001350654.1:p.Pro170ArgfsTer6
XM_011535984.2:c.2838del	XP_011534286.2:p.Pro947ArgfsTer6
XM_011535988.3:c.-20+15661del	XP_011534290.1:n.-20+15661del
XM_017011103.2:c.2838del	XP_016866592.1:p.Pro947ArgfsTer6
XM_017011104.1:c.2838del	XP_016866593.1:p.Pro947ArgfsTer6
XM_017011105.2:c.2838del	XP_016866594.1:p.Pro947ArgfsTer6
XM_017011106.2:c.2838del	XP_016866595.1:p.Pro947ArgfsTer6
XM_017011107.2:c.2658del	XP_016866596.1:p.Pro887ArgfsTer6
XR_002956289.1:n.2921del
NM_001363725.2:c.507del	NP_001350654.1:p.Pro170ArgfsTer6
NM_001371656.1:c.3045del	NP_001358585.1:p.Pro1016ArgfsTer6
NM_001374820.1:c.3045del	NP_001361749.1:p.Pro1016ArgfsTer6
NM_001374828.1:c.3006del MANE Select	NP_001361757.1:p.Pro1003ArgfsTer6
NM_017519.3:c.3006del	NP_059989.3:p.Pro1003ArgfsTer6