Canonical Allele Identifier: CA2680917440

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148830-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148833_157148835del , CM000668.2:g.157148833_157148835del	GRCh38
NC_000006.11:g.157469967_157469969del , CM000668.1:g.157469967_157469969del	GRCh37
NC_000006.10:g.157511659_157511661del	NCBI36
NG_032093.1:g.375904_375906del
NG_032093.2:g.375904_375906del
NG_066624.1:g.377808_377810del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2971_2973del	ENSP00000055163.8:p.Pro991del
ENST00000414678.8:c.2881_2883del	ENSP00000412835.3:p.Pro961del
ENST00000637015.2:c.2971_2973del	ENSP00000489729.2:p.Pro991del
ENST00000319584.11:c.985_987del	ENSP00000313006.7:p.Pro329del
ENST00000346085.10:c.3010_3012del	ENSP00000344546.5:p.Pro1004del
ENST00000350026.10:c.2722_2724del	ENSP00000055163.7:p.Pro908del
ENST00000414678.7:c.1129_1131del	ENSP00000412835.2:p.Pro377del
ENST00000452544.2:n.872_874del
ENST00000635849.1:c.292_294del	ENSP00000490948.1:p.Pro98del
ENST00000636426.1:n.105_107del
ENST00000636930.2:c.2971_2973del MANE Select	ENSP00000490491.2:p.Pro991del
ENST00000637015.1:c.210_212del
ENST00000637568.1:c.14_16del
ENST00000637810.1:c.472_474del	ENSP00000489636.1:p.Pro158del
ENST00000637904.1:c.472_474del	ENSP00000490550.1:p.Pro158del
ENST00000647938.1:c.2761_2763del	ENSP00000498155.1:p.Pro921del
ENST00000674190.1:n.1720_1722del
ENST00000319584.10:c.988_990del	ENSP00000313006.6:p.Pro330del
ENST00000346085.9:c.2761_2763del	ENSP00000344546.4:p.Pro921del
ENST00000350026.9:c.2722_2724del	ENSP00000055163.7:p.Pro908del
ENST00000414678.6:c.1129_1131del	ENSP00000412835.2:p.Pro377del
ENST00000452544.1:n.818_820del
ENST00000478761.3:c.44_46del
NM_017519.2:c.2722_2724del	NP_059989.2:p.Pro908del
NM_020732.3:c.2761_2763del	NP_065783.3:p.Pro921del
XM_005267069.3:c.2722_2724del	XP_005267126.2:p.Pro908del
XM_011535984.1:c.1672_1674del	XP_011534286.1:p.Pro558del
XM_011535985.1:c.1492_1494del	XP_011534287.1:p.Pro498del
XM_011535986.1:c.1252_1254del	XP_011534288.1:p.Pro418del
XM_011535987.1:c.871_873del	XP_011534289.1:p.Pro291del
XM_011535988.1:c.-20+15626_-20+15628del	XP_011534290.1:n.-20+15626_-20+15628del
NM_001346813.1:c.2722_2724del	NP_001333742.1:p.Pro908del
NM_001363725.1:c.472_474del	NP_001350654.1:p.Pro158del
XM_011535984.2:c.2803_2805del	XP_011534286.2:p.Pro935del
XM_011535988.3:c.-20+15626_-20+15628del	XP_011534290.1:n.-20+15626_-20+15628del
XM_017011103.2:c.2803_2805del	XP_016866592.1:p.Pro935del
XM_017011104.1:c.2803_2805del	XP_016866593.1:p.Pro935del
XM_017011105.2:c.2803_2805del	XP_016866594.1:p.Pro935del
XM_017011106.2:c.2803_2805del	XP_016866595.1:p.Pro935del
XM_017011107.2:c.2623_2625del	XP_016866596.1:p.Pro875del
XR_002956289.1:n.2886_2888del
NM_001363725.2:c.472_474del	NP_001350654.1:p.Pro158del
NM_001371656.1:c.3010_3012del	NP_001358585.1:p.Pro1004del
NM_001374820.1:c.3010_3012del	NP_001361749.1:p.Pro1004del
NM_001374828.1:c.2971_2973del MANE Select	NP_001361757.1:p.Pro991del
NM_017519.3:c.2971_2973del	NP_059989.3:p.Pro991del