Canonical Allele Identifier: CA2695207304

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148875dup , CM000668.2:g.157148875dup	GRCh38
NC_000006.11:g.157470009dup , CM000668.1:g.157470009dup	GRCh37
NC_000006.10:g.157511701dup	NCBI36
NG_032093.1:g.375946dup
NG_032093.2:g.375946dup
NG_066624.1:g.377850dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3013dup	ENSP00000055163.8:p.Met1005AsnfsTer7
ENST00000414678.8:c.2923dup	ENSP00000412835.3:p.Met975AsnfsTer7
ENST00000637015.2:c.3013dup	ENSP00000489729.2:p.Met1005AsnfsTer7
ENST00000319584.11:c.1027dup	ENSP00000313006.7:p.Met343AsnfsTer7
ENST00000346085.10:c.3052dup	ENSP00000344546.5:p.Met1018AsnfsTer7
ENST00000350026.10:c.2764dup	ENSP00000055163.7:p.Met922AsnfsTer7
ENST00000414678.7:c.1171dup	ENSP00000412835.2:p.Met391AsnfsTer7
ENST00000452544.2:n.914dup
ENST00000635849.1:c.334dup	ENSP00000490948.1:p.Met112AsnfsTer7
ENST00000636426.1:n.147dup
ENST00000636930.2:c.3013dup MANE Select	ENSP00000490491.2:p.Met1005AsnfsTer7
ENST00000637015.1:c.252dup
ENST00000637568.1:c.56dup
ENST00000637810.1:c.514dup	ENSP00000489636.1:p.Met172AsnfsTer7
ENST00000637904.1:c.514dup	ENSP00000490550.1:p.Met172AsnfsTer7
ENST00000647938.1:c.2803dup	ENSP00000498155.1:p.Met935AsnfsTer7
ENST00000674190.1:n.1762dup
ENST00000319584.10:c.1030dup	ENSP00000313006.6:p.Met344AsnfsTer7
ENST00000346085.9:c.2803dup	ENSP00000344546.4:p.Met935AsnfsTer7
ENST00000350026.9:c.2764dup	ENSP00000055163.7:p.Met922AsnfsTer7
ENST00000414678.6:c.1171dup	ENSP00000412835.2:p.Met391AsnfsTer7
ENST00000452544.1:n.860dup
ENST00000478761.3:c.86dup
NM_017519.2:c.2764dup	NP_059989.2:p.Met922AsnfsTer7
NM_020732.3:c.2803dup	NP_065783.3:p.Met935AsnfsTer7
XM_005267069.3:c.2764dup	XP_005267126.2:p.Met922AsnfsTer7
XM_011535984.1:c.1714dup	XP_011534286.1:p.Met572AsnfsTer7
XM_011535985.1:c.1534dup	XP_011534287.1:p.Met512AsnfsTer7
XM_011535986.1:c.1294dup	XP_011534288.1:p.Met432AsnfsTer7
XM_011535987.1:c.913dup	XP_011534289.1:p.Met305AsnfsTer7
XM_011535988.1:c.-20+15668dup	XP_011534290.1:n.-20+15668dup
NM_001346813.1:c.2764dup	NP_001333742.1:p.Met922AsnfsTer7
NM_001363725.1:c.514dup	NP_001350654.1:p.Met172AsnfsTer7
XM_011535984.2:c.2845dup	XP_011534286.2:p.Met949AsnfsTer7
XM_011535988.3:c.-20+15668dup	XP_011534290.1:n.-20+15668dup
XM_017011103.2:c.2845dup	XP_016866592.1:p.Met949AsnfsTer7
XM_017011104.1:c.2845dup	XP_016866593.1:p.Met949AsnfsTer7
XM_017011105.2:c.2845dup	XP_016866594.1:p.Met949AsnfsTer7
XM_017011106.2:c.2845dup	XP_016866595.1:p.Met949AsnfsTer7
XM_017011107.2:c.2665dup	XP_016866596.1:p.Met889AsnfsTer7
XR_002956289.1:n.2928dup
NM_001363725.2:c.514dup	NP_001350654.1:p.Met172AsnfsTer7
NM_001371656.1:c.3052dup	NP_001358585.1:p.Met1018AsnfsTer7
NM_001374820.1:c.3052dup	NP_001361749.1:p.Met1018AsnfsTer7
NM_001374828.1:c.3013dup MANE Select	NP_001361757.1:p.Met1005AsnfsTer7
NM_017519.3:c.3013dup	NP_059989.3:p.Met1005AsnfsTer7