Canonical Allele Identifier: CA2695207236

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148644_157148645delinsCTGG , CM000668.2:g.157148644_157148645delinsCTGG	GRCh38
NC_000006.11:g.157469778_157469779delinsCTGG , CM000668.1:g.157469778_157469779delinsCTGG	GRCh37
NC_000006.10:g.157511470_157511471delinsCTGG	NCBI36
NG_032093.1:g.375715_375716delinsCTGG
NG_032093.2:g.375715_375716delinsCTGG
NG_066624.1:g.377619_377620delinsCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2782_2783delinsCTGG	ENSP00000055163.8:p.Ala928LeufsTer?
ENST00000414678.8:c.2692_2693delinsCTGG	ENSP00000412835.3:p.Ala898LeufsTer?
ENST00000637015.2:c.2782_2783delinsCTGG	ENSP00000489729.2:p.Ala928LeufsTer?
ENST00000319584.11:c.796_797delinsCTGG	ENSP00000313006.7:p.Ala266LeufsTer?
ENST00000346085.10:c.2821_2822delinsCTGG	ENSP00000344546.5:p.Ala941LeufsTer?
ENST00000350026.10:c.2533_2534delinsCTGG	ENSP00000055163.7:p.Ala845LeufsTer?
ENST00000414678.7:c.940_941delinsCTGG	ENSP00000412835.2:p.Ala314LeufsTer?
ENST00000452544.2:n.683_684delinsCTGG
ENST00000635849.1:c.103_104delinsCTGG	ENSP00000490948.1:p.Ala35LeufsTer?
ENST00000636930.2:c.2782_2783delinsCTGG MANE Select	ENSP00000490491.2:p.Ala928LeufsTer?
ENST00000637015.1:c.21_22delinsCTGG
ENST00000637810.1:c.283_284delinsCTGG	ENSP00000489636.1:p.Ala95LeufsTer?
ENST00000637904.1:c.283_284delinsCTGG	ENSP00000490550.1:p.Ala95LeufsTer?
ENST00000647938.1:c.2572_2573delinsCTGG	ENSP00000498155.1:p.Ala858LeufsTer?
ENST00000674190.1:n.1531_1532delinsCTGG
ENST00000319584.10:c.799_800delinsCTGG	ENSP00000313006.6:p.Ala267LeufsTer?
ENST00000346085.9:c.2572_2573delinsCTGG	ENSP00000344546.4:p.Ala858LeufsTer?
ENST00000350026.9:c.2533_2534delinsCTGG	ENSP00000055163.7:p.Ala845LeufsTer?
ENST00000414678.6:c.940_941delinsCTGG	ENSP00000412835.2:p.Ala314LeufsTer?
ENST00000452544.1:n.629_630delinsCTGG
NM_017519.2:c.2533_2534delinsCTGG	NP_059989.2:p.Ala845LeufsTer?
NM_020732.3:c.2572_2573delinsCTGG	NP_065783.3:p.Ala858LeufsTer?
XM_005267069.3:c.2533_2534delinsCTGG	XP_005267126.2:p.Ala845LeufsTer?
XM_011535984.1:c.1483_1484delinsCTGG	XP_011534286.1:p.Ala495LeufsTer?
XM_011535985.1:c.1303_1304delinsCTGG	XP_011534287.1:p.Ala435LeufsTer?
XM_011535986.1:c.1063_1064delinsCTGG	XP_011534288.1:p.Ala355LeufsTer?
XM_011535987.1:c.682_683delinsCTGG	XP_011534289.1:p.Ala228LeufsTer?
XM_011535988.1:c.-20+15437_-20+15438delinsCTGG	XP_011534290.1:n.-20+15437_-20+15438delinsCTGG
NM_001346813.1:c.2533_2534delinsCTGG	NP_001333742.1:p.Ala845LeufsTer?
NM_001363725.1:c.283_284delinsCTGG	NP_001350654.1:p.Ala95LeufsTer?
XM_011535984.2:c.2614_2615delinsCTGG	XP_011534286.2:p.Ala872LeufsTer?
XM_011535988.3:c.-20+15437_-20+15438delinsCTGG	XP_011534290.1:n.-20+15437_-20+15438delinsCTGG
XM_017011103.2:c.2614_2615delinsCTGG	XP_016866592.1:p.Ala872LeufsTer?
XM_017011104.1:c.2614_2615delinsCTGG	XP_016866593.1:p.Ala872LeufsTer?
XM_017011105.2:c.2614_2615delinsCTGG	XP_016866594.1:p.Ala872LeufsTer?
XM_017011106.2:c.2614_2615delinsCTGG	XP_016866595.1:p.Ala872LeufsTer?
XM_017011107.2:c.2434_2435delinsCTGG	XP_016866596.1:p.Ala812LeufsTer?
XR_002956289.1:n.2697_2698delinsCTGG
NM_001363725.2:c.283_284delinsCTGG	NP_001350654.1:p.Ala95LeufsTer?
NM_001371656.1:c.2821_2822delinsCTGG	NP_001358585.1:p.Ala941LeufsTer?
NM_001374820.1:c.2821_2822delinsCTGG	NP_001361749.1:p.Ala941LeufsTer?
NM_001374828.1:c.2782_2783delinsCTGG MANE Select	NP_001361757.1:p.Ala928LeufsTer?
NM_017519.3:c.2782_2783delinsCTGG	NP_059989.3:p.Ala928LeufsTer?