Canonical Allele Identifier: CA339168557

Gene: ARID1A

Linked Data

• ClinVar Variation Id: 427049
• ClinVar RCV Id: RCV000489657
• dbSNP Id: rs1085307923
• MyVariant Identifiers: chr1:g.27099885G>A (hg19) ; chr1:g.26773394G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26773394G>A , CM000663.2:g.26773394G>A	GRCh38
NC_000001.10:g.27099885G>A , CM000663.1:g.27099885G>A	GRCh37
NC_000001.9:g.26972472G>A	NCBI36
NG_029965.1:g.82364G>A , LRG_875:g.82364G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.3764G>A MANE Select	ENSP00000320485.7:p.Gly1255Glu
ENST00000374152.7:c.2615G>A	ENSP00000363267.2:p.Gly872Glu
ENST00000430799.7:c.2612G>A	ENSP00000390317.3:p.Gly871Glu
ENST00000466382.2:c.73G>A
ENST00000636072.1:n.74G>A
ENST00000636219.1:c.2618G>A	ENSP00000489842.1:p.Gly873Glu
ENST00000636794.1:n.70G>A
ENST00000324856.11:c.3764G>A	ENSP00000320485.7:p.Gly1255Glu
ENST00000374152.6:c.2615G>A	ENSP00000363267.2:p.Gly872Glu
ENST00000430799.6:c.453G>A
ENST00000457599.6:c.3764G>A	ENSP00000387636.2:p.Gly1255Glu
ENST00000466382.1:c.73G>A
ENST00000615191.4:c.2612G>A	ENSP00000478955.1:p.Gly871Glu
NM_006015.4:c.3764G>A , LRG_875t1:c.3764G>A	NP_006006.3:p.Gly1255Glu
NM_139135.2:c.3764G>A	NP_624361.1:p.Gly1255Glu
NM_006015.5:c.3764G>A	NP_006006.3:p.Gly1255Glu
NM_139135.3:c.3764G>A	NP_624361.1:p.Gly1255Glu
NM_006015.6:c.3764G>A MANE Select	NP_006006.3:p.Gly1255Glu
NM_139135.4:c.3764G>A	NP_624361.1:p.Gly1255Glu