Canonical Allele Identifier: CA416989334

Gene: ARID1A

Linked Data

• dbSNP Id: rs1015322780
• gnomAD v2: 1-27023140-TGGC-T
• gnomAD v3: 1-26696649-TGGC-T
• gnomAD v4: 1-26696649-TGGC-T
• MyVariant Identifiers: chr1:g.27023141_27023143del (hg19) ; chr1:g.27023152_27023158delinsAGCC (hg19) ; chr1:g.26696661_26696667delinsAGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696661_26696663del , CM000663.2:g.26696661_26696663del	GRCh38
NC_000001.10:g.27023152_27023154del , CM000663.1:g.27023152_27023154del	GRCh37
NC_000001.9:g.26895739_26895741del	NCBI36
NG_029965.1:g.5631_5633del , LRG_875:g.5631_5633del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.258_260del MANE Select	ENSP00000320485.7:p.Gly87del
ENST00000430799.7:c.-13+3044_-13+3046del	ENSP00000390317.3:n.-13+3044_-13+3046del
ENST00000637465.1:c.-13+561_-13+563del	ENSP00000490650.1:n.-13+561_-13+563del
ENST00000324856.11:c.258_260del	ENSP00000320485.7:p.Gly87del
ENST00000457599.6:c.258_260del	ENSP00000387636.2:p.Gly87del
NM_006015.4:c.258_260del , LRG_875t1:c.258_260del	NP_006006.3:p.Gly87del
NM_139135.2:c.258_260del	NP_624361.1:p.Gly87del
NM_006015.5:c.258_260del	NP_006006.3:p.Gly87del
NM_139135.3:c.258_260del	NP_624361.1:p.Gly87del
NM_006015.6:c.258_260del MANE Select	NP_006006.3:p.Gly87del
NM_139135.4:c.258_260del	NP_624361.1:p.Gly87del