Canonical Allele Identifier: CA2578780307

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157180940del , CM000668.2:g.157180940del	GRCh38
NC_000006.11:g.157502074del , CM000668.1:g.157502074del	GRCh37
NC_000006.10:g.157543766del	NCBI36
NG_032093.1:g.408011del
NG_032093.2:g.408011del
NG_066624.1:g.409915del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3346-29del	ENSP00000055163.8:n.3346-29del
ENST00000414678.8:c.3415-29del	ENSP00000412835.3:n.3415-29del
ENST00000637015.2:c.3634-29del	ENSP00000489729.2:n.3634-29del
ENST00000319584.11:c.1519-29del	ENSP00000313006.7:n.1519-29del
ENST00000346085.10:c.3385-29del	ENSP00000344546.5:n.3385-29del
ENST00000350026.10:c.3097-29del	ENSP00000055163.7:n.3097-29del
ENST00000414678.7:c.1663-29del	ENSP00000412835.2:n.1663-29del
ENST00000478761.4:n.293-29del
ENST00000635849.1:c.826-29del	ENSP00000490948.1:n.826-29del
ENST00000635957.1:c.460-29del	ENSP00000490385.1:n.460-29del
ENST00000636930.2:c.3505-29del MANE Select	ENSP00000490491.2:n.3505-29del
ENST00000636940.1:n.1502-29del
ENST00000637015.1:c.873-29del
ENST00000637568.1:c.787-29del
ENST00000637741.1:n.171-29del
ENST00000637810.1:c.847-29del	ENSP00000489636.1:n.847-29del
ENST00000637904.1:c.1006-29del	ENSP00000490550.1:n.1006-29del
ENST00000647938.1:c.3136-29del	ENSP00000498155.1:n.3136-29del
ENST00000319584.10:c.1522-29del	ENSP00000313006.6:n.1522-29del
ENST00000346085.9:c.3136-29del	ENSP00000344546.4:n.3136-29del
ENST00000350026.9:c.3097-29del	ENSP00000055163.7:n.3097-29del
ENST00000400790.3:c.298-29del	ENSP00000383596.3:n.298-29del
ENST00000414678.6:c.1663-29del	ENSP00000412835.2:n.1663-29del
ENST00000478761.3:c.707-29del
NM_017519.2:c.3097-29del	NP_059989.2:n.3097-29del
NM_020732.3:c.3136-29del	NP_065783.3:n.3136-29del
XM_005267069.3:c.3256-29del	XP_005267126.2:n.3256-29del
XM_011535984.1:c.2335-29del	XP_011534286.1:n.2335-29del
XM_011535985.1:c.2155-29del	XP_011534287.1:n.2155-29del
XM_011535986.1:c.1915-29del	XP_011534288.1:n.1915-29del
XM_011535987.1:c.1534-29del	XP_011534289.1:n.1534-29del
XM_011535988.1:c.397-29del	XP_011534290.1:n.397-29del
NM_001346813.1:c.3256-29del	NP_001333742.1:n.3256-29del
NM_001363725.1:c.1006-29del	NP_001350654.1:n.1006-29del
XM_011535984.2:c.3466-29del	XP_011534286.2:n.3466-29del
XM_011535988.3:c.397-29del	XP_011534290.1:n.397-29del
XM_017011103.2:c.3367-29del	XP_016866592.1:n.3367-29del
XM_017011104.1:c.3337-29del	XP_016866593.1:n.3337-29del
XM_017011105.2:c.3307-29del	XP_016866594.1:n.3307-29del
XM_017011106.2:c.3178-29del	XP_016866595.1:n.3178-29del
XM_017011107.2:c.3157-29del	XP_016866596.1:n.3157-29del
XR_002956289.1:n.3549-29del
NM_001363725.2:c.1006-29del	NP_001350654.1:n.1006-29del
NM_001371656.1:c.3385-29del	NP_001358585.1:n.3385-29del
NM_001374820.1:c.3385-29del	NP_001361749.1:n.3385-29del
NM_001374828.1:c.3505-29del MANE Select	NP_001361757.1:n.3505-29del
NM_017519.3:c.3346-29del	NP_059989.3:n.3346-29del