Canonical Allele Identifier: CA2680891549

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201391-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201396del , CM000668.2:g.157201396del	GRCh38
NC_000006.11:g.157522530del , CM000668.1:g.157522530del	GRCh37
NC_000006.10:g.157564222del	NCBI36
NG_032093.1:g.428467del
NG_032093.2:g.428467del
NG_066624.1:g.430371del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5012del	ENSP00000055163.8:p.Pro1671GlnfsTer13
ENST00000414678.8:c.5081del	ENSP00000412835.3:p.Pro1694GlnfsTer13
ENST00000637015.2:c.5300del	ENSP00000489729.2:p.Pro1767GlnfsTer13
ENST00000346085.10:c.5051del	ENSP00000344546.5:p.Pro1684GlnfsTer13
ENST00000350026.10:c.4763del	ENSP00000055163.7:p.Pro1588GlnfsTer13
ENST00000414678.7:c.3329del	ENSP00000412835.2:p.Pro1110GlnfsTer13
ENST00000635849.1:c.2492del	ENSP00000490948.1:p.Pro831GlnfsTer13
ENST00000635957.1:c.2123del	ENSP00000490385.1:p.Pro708GlnfsTer13
ENST00000636227.1:n.3634del
ENST00000636254.1:n.1091del
ENST00000636930.2:c.5171del MANE Select	ENSP00000490491.2:p.Pro1724GlnfsTer13
ENST00000636940.1:n.3168del
ENST00000637015.1:c.2539del
ENST00000637568.1:c.2453del
ENST00000637741.1:n.1837del
ENST00000637810.1:c.2513del	ENSP00000489636.1:p.Pro838GlnfsTer13
ENST00000637904.1:c.2672del	ENSP00000490550.1:p.Pro891GlnfsTer13
ENST00000647938.1:c.4802del	ENSP00000498155.1:p.Pro1601GlnfsTer13
ENST00000346085.9:c.4802del	ENSP00000344546.4:p.Pro1601GlnfsTer13
ENST00000350026.9:c.4763del	ENSP00000055163.7:p.Pro1588GlnfsTer13
ENST00000414678.6:c.3329del	ENSP00000412835.2:p.Pro1110GlnfsTer13
NM_017519.2:c.4763del	NP_059989.2:p.Pro1588GlnfsTer13
NM_020732.3:c.4802del	NP_065783.3:p.Pro1601GlnfsTer13
XM_005267069.3:c.4922del	XP_005267126.2:p.Pro1641GlnfsTer13
XM_011535984.1:c.4001del	XP_011534286.1:p.Pro1334GlnfsTer13
XM_011535985.1:c.3821del	XP_011534287.1:p.Pro1274GlnfsTer13
XM_011535986.1:c.3581del	XP_011534288.1:p.Pro1194GlnfsTer13
XM_011535987.1:c.3200del	XP_011534289.1:p.Pro1067GlnfsTer13
XM_011535988.1:c.2063del	XP_011534290.1:p.Pro688GlnfsTer13
NM_001346813.1:c.4922del	NP_001333742.1:p.Pro1641GlnfsTer13
NM_001363725.1:c.2672del	NP_001350654.1:p.Pro891GlnfsTer13
XM_011535984.2:c.5132del	XP_011534286.2:p.Pro1711GlnfsTer13
XM_011535988.3:c.2063del	XP_011534290.1:p.Pro688GlnfsTer13
XM_017011103.2:c.5033del	XP_016866592.1:p.Pro1678GlnfsTer13
XM_017011104.1:c.5003del	XP_016866593.1:p.Pro1668GlnfsTer13
XM_017011105.2:c.4973del	XP_016866594.1:p.Pro1658GlnfsTer13
XM_017011106.2:c.4844del	XP_016866595.1:p.Pro1615GlnfsTer13
XM_017011107.2:c.4823del	XP_016866596.1:p.Pro1608GlnfsTer13
XR_002956289.1:n.5118del
NM_001363725.2:c.2672del	NP_001350654.1:p.Pro891GlnfsTer13
NM_001371656.1:c.5051del	NP_001358585.1:p.Pro1684GlnfsTer13
NM_001374820.1:c.5051del	NP_001361749.1:p.Pro1684GlnfsTer13
NM_001374828.1:c.5171del MANE Select	NP_001361757.1:p.Pro1724GlnfsTer13
NM_017519.3:c.5012del	NP_059989.3:p.Pro1671GlnfsTer13