Canonical Allele Identifier: CA10584013

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 242864
• ClinVar RCV Id: RCV000234906
• dbSNP Id: rs879253745
• MyVariant Identifiers: chr6:g.157502175_157502176del (hg19) ; chr6:g.157181041_157181042del (hg38)
• PubMed: PMID:24674232

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181041_157181042del , CM000668.2:g.157181041_157181042del	GRCh38
NC_000006.11:g.157502175_157502176del , CM000668.1:g.157502175_157502176del	GRCh37
NC_000006.10:g.157543867_157543868del	NCBI36
NG_032093.1:g.408112_408113del
NG_032093.2:g.408112_408113del
NG_066624.1:g.410016_410017del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3418_3419del	ENSP00000055163.8:p.Lys1140AlafsTer?
ENST00000414678.8:c.3487_3488del	ENSP00000412835.3:p.Lys1163AlafsTer?
ENST00000637015.2:c.3706_3707del	ENSP00000489729.2:p.Lys1236AlafsTer?
ENST00000319584.11:c.1591_1592del	ENSP00000313006.7:p.Lys531AlafsTer?
ENST00000346085.10:c.3457_3458del	ENSP00000344546.5:p.Lys1153AlafsTer?
ENST00000350026.10:c.3169_3170del	ENSP00000055163.7:p.Lys1057AlafsTer?
ENST00000414678.7:c.1735_1736del	ENSP00000412835.2:p.Lys579AlafsTer?
ENST00000635849.1:c.898_899del	ENSP00000490948.1:p.Lys300AlafsTer?
ENST00000635957.1:c.532_533del	ENSP00000490385.1:p.Lys178AlafsTer?
ENST00000636930.2:c.3577_3578del MANE Select	ENSP00000490491.2:p.Lys1193AlafsTer?
ENST00000636940.1:n.1574_1575del
ENST00000637015.1:c.945_946del
ENST00000637568.1:c.859_860del
ENST00000637741.1:n.243_244del
ENST00000637810.1:c.919_920del	ENSP00000489636.1:p.Lys307AlafsTer?
ENST00000637904.1:c.1078_1079del	ENSP00000490550.1:p.Lys360AlafsTer?
ENST00000647938.1:c.3208_3209del	ENSP00000498155.1:p.Lys1070AlafsTer?
ENST00000319584.10:c.1594_1595del	ENSP00000313006.6:p.Lys532AlafsTer?
ENST00000346085.9:c.3208_3209del	ENSP00000344546.4:p.Lys1070AlafsTer?
ENST00000350026.9:c.3169_3170del	ENSP00000055163.7:p.Lys1057AlafsTer?
ENST00000400790.3:c.370_371del	ENSP00000383596.3:p.Lys124AlafsTer?
ENST00000414678.6:c.1735_1736del	ENSP00000412835.2:p.Lys579AlafsTer?
ENST00000478761.3:c.779_780del
NM_017519.2:c.3169_3170del	NP_059989.2:p.Lys1057AlafsTer?
NM_020732.3:c.3208_3209del	NP_065783.3:p.Lys1070AlafsTer?
XM_005267069.3:c.3328_3329del	XP_005267126.2:p.Lys1110AlafsTer?
XM_011535984.1:c.2407_2408del	XP_011534286.1:p.Lys803AlafsTer?
XM_011535985.1:c.2227_2228del	XP_011534287.1:p.Lys743AlafsTer?
XM_011535986.1:c.1987_1988del	XP_011534288.1:p.Lys663AlafsTer?
XM_011535987.1:c.1606_1607del	XP_011534289.1:p.Lys536AlafsTer?
XM_011535988.1:c.469_470del	XP_011534290.1:p.Lys157AlafsTer?
NM_001346813.1:c.3328_3329del	NP_001333742.1:p.Lys1110AlafsTer?
NM_001363725.1:c.1078_1079del	NP_001350654.1:p.Lys360AlafsTer?
XM_011535984.2:c.3538_3539del	XP_011534286.2:p.Lys1180AlafsTer?
XM_011535988.3:c.469_470del	XP_011534290.1:p.Lys157AlafsTer?
XM_017011103.2:c.3439_3440del	XP_016866592.1:p.Lys1147AlafsTer?
XM_017011104.1:c.3409_3410del	XP_016866593.1:p.Lys1137AlafsTer?
XM_017011105.2:c.3379_3380del	XP_016866594.1:p.Lys1127AlafsTer?
XM_017011106.2:c.3250_3251del	XP_016866595.1:p.Lys1084AlafsTer?
XM_017011107.2:c.3229_3230del	XP_016866596.1:p.Lys1077AlafsTer?
XR_002956289.1:n.3621_3622del
NM_001363725.2:c.1078_1079del	NP_001350654.1:p.Lys360AlafsTer?
NM_001371656.1:c.3457_3458del	NP_001358585.1:p.Lys1153AlafsTer?
NM_001374820.1:c.3457_3458del	NP_001361749.1:p.Lys1153AlafsTer?
NM_001374828.1:c.3577_3578del MANE Select	NP_001361757.1:p.Lys1193AlafsTer?
NM_017519.3:c.3418_3419del	NP_059989.3:p.Lys1140AlafsTer?