Canonical Allele Identifier: CA339184489

Gene: ARID1A

Linked Data

• gnomAD v4: 1-26779170-C-A
• MyVariant Identifiers: chr1:g.27105661C>A (hg19) ; chr1:g.26779170C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779170C>A , CM000663.2:g.26779170C>A	GRCh38
NC_000001.10:g.27105661C>A , CM000663.1:g.27105661C>A	GRCh37
NC_000001.9:g.26978248C>A	NCBI36
NG_029965.1:g.88140C>A , LRG_875:g.88140C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5272C>A MANE Select	ENSP00000320485.7:p.Pro1758Thr
ENST00000374152.7:c.4123C>A	ENSP00000363267.2:p.Pro1375Thr
ENST00000430799.7:c.4120C>A	ENSP00000390317.3:p.Pro1374Thr
ENST00000466382.2:c.689C>A
ENST00000636219.1:c.4126C>A	ENSP00000489842.1:p.Pro1376Thr
ENST00000637788.1:n.1072C>A
ENST00000324856.11:c.5272C>A	ENSP00000320485.7:p.Pro1758Thr
ENST00000374152.6:c.4123C>A	ENSP00000363267.2:p.Pro1375Thr
ENST00000430799.6:c.1961C>A
ENST00000457599.6:c.4621C>A	ENSP00000387636.2:p.Pro1541Thr
ENST00000466382.1:c.689C>A
ENST00000532781.1:c.770C>A
NM_006015.4:c.5272C>A , LRG_875t1:c.5272C>A	NP_006006.3:p.Pro1758Thr
NM_139135.2:c.4621C>A	NP_624361.1:p.Pro1541Thr
NM_006015.5:c.5272C>A	NP_006006.3:p.Pro1758Thr
NM_139135.3:c.4621C>A	NP_624361.1:p.Pro1541Thr
NM_006015.6:c.5272C>A MANE Select	NP_006006.3:p.Pro1758Thr
NM_139135.4:c.4621C>A	NP_624361.1:p.Pro1541Thr