Canonical Allele Identifier: CA2582341907

Gene: ARID1A

Linked Data

• ClinVar Variation Id: 2582276
• ClinVar RCV Id: RCV003332977

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26767906dup , CM000663.2:g.26767906dup	GRCh38
NC_000001.10:g.27094397dup , CM000663.1:g.27094397dup	GRCh37
NC_000001.9:g.26966984dup	NCBI36
NG_029965.1:g.76876dup , LRG_875:g.76876dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.3105dup MANE Select	ENSP00000320485.7:p.Met1036HisfsTer11
ENST00000374152.7:c.1956dup	ENSP00000363267.2:p.Met653HisfsTer11
ENST00000430291.2:n.414dup
ENST00000430799.7:c.1956dup	ENSP00000390317.3:p.Met653HisfsTer11
ENST00000636219.1:c.1962dup	ENSP00000489842.1:p.Met655HisfsTer11
ENST00000324856.11:c.3105dup	ENSP00000320485.7:p.Met1036HisfsTer11
ENST00000374152.6:c.1956dup	ENSP00000363267.2:p.Met653HisfsTer11
ENST00000430291.1:n.414dup
ENST00000457599.6:c.3105dup	ENSP00000387636.2:p.Met1036HisfsTer11
ENST00000615191.4:c.1953dup	ENSP00000478955.1:p.Met652HisfsTer11
NM_006015.4:c.3105dup , LRG_875t1:c.3105dup	NP_006006.3:p.Met1036HisfsTer11
NM_139135.2:c.3105dup	NP_624361.1:p.Met1036HisfsTer11
NM_006015.5:c.3105dup	NP_006006.3:p.Met1036HisfsTer11
NM_139135.3:c.3105dup	NP_624361.1:p.Met1036HisfsTer11
NM_006015.6:c.3105dup MANE Select	NP_006006.3:p.Met1036HisfsTer11
NM_139135.4:c.3105dup	NP_624361.1:p.Met1036HisfsTer11