Canonical Allele Identifier: CA339166598

Gene: ARID1A

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26772633G>A , CM000663.2:g.26772633G>A	GRCh38
NC_000001.10:g.27099124G>A , CM000663.1:g.27099124G>A	GRCh37
NC_000001.9:g.26971711G>A	NCBI36
NG_029965.1:g.81603G>A , LRG_875:g.81603G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.3539+1G>A MANE Select	ENSP00000320485.7:n.3539+1G>A
ENST00000374152.7:c.2390+1G>A	ENSP00000363267.2:n.2390+1G>A
ENST00000430799.7:c.2390+1G>A	ENSP00000390317.3:n.2390+1G>A
ENST00000636219.1:c.2396+1G>A	ENSP00000489842.1:n.2396+1G>A
ENST00000324856.11:c.3539+1G>A	ENSP00000320485.7:n.3539+1G>A
ENST00000374152.6:c.2390+1G>A	ENSP00000363267.2:n.2390+1G>A
ENST00000430799.6:c.231+1G>A
ENST00000457599.6:c.3539+1G>A	ENSP00000387636.2:n.3539+1G>A
ENST00000615191.4:c.2387+1G>A	ENSP00000478955.1:n.2387+1G>A
NM_006015.4:c.3539+1G>A , LRG_875t1:c.3539+1G>A	NP_006006.3:n.3539+1G>A
NM_139135.2:c.3539+1G>A	NP_624361.1:n.3539+1G>A
NM_006015.5:c.3539+1G>A	NP_006006.3:n.3539+1G>A
NM_139135.3:c.3539+1G>A	NP_624361.1:n.3539+1G>A
NM_006015.6:c.3539+1G>A MANE Select	NP_006006.3:n.3539+1G>A
NM_139135.4:c.3539+1G>A	NP_624361.1:n.3539+1G>A