Canonical Allele Identifier: CA915944780

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 817117
• ClinVar RCV Id: RCV001008220
• dbSNP Id: rs1583464090

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181173del , CM000668.2:g.157181173del	GRCh38
NC_000006.11:g.157502307del , CM000668.1:g.157502307del	GRCh37
NC_000006.10:g.157543999del	NCBI36
NG_032093.1:g.408244del
NG_032093.2:g.408244del
NG_066624.1:g.410148del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3550del	ENSP00000055163.8:p.Ala1184ProfsTer16
ENST00000414678.8:c.3619del	ENSP00000412835.3:p.Ala1207ProfsTer16
ENST00000637015.2:c.3838del	ENSP00000489729.2:p.Ala1280ProfsTer16
ENST00000319584.11:c.1723del	ENSP00000313006.7:p.Ala575ProfsTer16
ENST00000346085.10:c.3589del	ENSP00000344546.5:p.Ala1197ProfsTer16
ENST00000350026.10:c.3301del	ENSP00000055163.7:p.Ala1101ProfsTer16
ENST00000414678.7:c.1867del	ENSP00000412835.2:p.Ala623ProfsTer16
ENST00000635849.1:c.1030del	ENSP00000490948.1:p.Ala344ProfsTer16
ENST00000635957.1:c.664del	ENSP00000490385.1:p.Ala222ProfsTer16
ENST00000636930.2:c.3709del MANE Select	ENSP00000490491.2:p.Ala1237ProfsTer16
ENST00000636940.1:n.1706del
ENST00000637015.1:c.1077del
ENST00000637568.1:c.991del
ENST00000637741.1:n.375del
ENST00000637810.1:c.1051del	ENSP00000489636.1:p.Ala351ProfsTer16
ENST00000637904.1:c.1210del	ENSP00000490550.1:p.Ala404ProfsTer16
ENST00000647938.1:c.3340del	ENSP00000498155.1:p.Ala1114ProfsTer16
ENST00000319584.10:c.1726del	ENSP00000313006.6:p.Ala576ProfsTer16
ENST00000346085.9:c.3340del	ENSP00000344546.4:p.Ala1114ProfsTer16
ENST00000350026.9:c.3301del	ENSP00000055163.7:p.Ala1101ProfsTer16
ENST00000400790.3:c.502del	ENSP00000383596.3:p.Ala168ProfsTer16
ENST00000414678.6:c.1867del	ENSP00000412835.2:p.Ala623ProfsTer16
ENST00000478761.3:c.911del
NM_017519.2:c.3301del	NP_059989.2:p.Ala1101ProfsTer16
NM_020732.3:c.3340del	NP_065783.3:p.Ala1114ProfsTer16
XM_005267069.3:c.3460del	XP_005267126.2:p.Ala1154ProfsTer16
XM_011535984.1:c.2539del	XP_011534286.1:p.Ala847ProfsTer16
XM_011535985.1:c.2359del	XP_011534287.1:p.Ala787ProfsTer16
XM_011535986.1:c.2119del	XP_011534288.1:p.Ala707ProfsTer16
XM_011535987.1:c.1738del	XP_011534289.1:p.Ala580ProfsTer16
XM_011535988.1:c.601del	XP_011534290.1:p.Ala201ProfsTer16
NM_001346813.1:c.3460del	NP_001333742.1:p.Ala1154ProfsTer16
NM_001363725.1:c.1210del	NP_001350654.1:p.Ala404ProfsTer16
XM_011535984.2:c.3670del	XP_011534286.2:p.Ala1224ProfsTer16
XM_011535988.3:c.601del	XP_011534290.1:p.Ala201ProfsTer16
XM_017011103.2:c.3571del	XP_016866592.1:p.Ala1191ProfsTer16
XM_017011104.1:c.3541del	XP_016866593.1:p.Ala1181ProfsTer16
XM_017011105.2:c.3511del	XP_016866594.1:p.Ala1171ProfsTer16
XM_017011106.2:c.3382del	XP_016866595.1:p.Ala1128ProfsTer16
XM_017011107.2:c.3361del	XP_016866596.1:p.Ala1121ProfsTer16
XR_002956289.1:n.3753del
NM_001363725.2:c.1210del	NP_001350654.1:p.Ala404ProfsTer16
NM_001371656.1:c.3589del	NP_001358585.1:p.Ala1197ProfsTer16
NM_001374820.1:c.3589del	NP_001361749.1:p.Ala1197ProfsTer16
NM_001374828.1:c.3709del MANE Select	NP_001361757.1:p.Ala1237ProfsTer16
NM_017519.3:c.3550del	NP_059989.3:p.Ala1184ProfsTer16