Canonical Allele Identifier: CA339184977

Gene: ARID1A

Linked Data

• dbSNP Id: rs1160398471
• MyVariant Identifiers: chr1:g.27105752T>A (hg19) ; chr1:g.26779261T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779261T>A , CM000663.2:g.26779261T>A	GRCh38
NC_000001.10:g.27105752T>A , CM000663.1:g.27105752T>A	GRCh37
NC_000001.9:g.26978339T>A	NCBI36
NG_029965.1:g.88231T>A , LRG_875:g.88231T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5363T>A MANE Select	ENSP00000320485.7:p.Ile1788Lys
ENST00000374152.7:c.4214T>A	ENSP00000363267.2:p.Ile1405Lys
ENST00000430799.7:c.4211T>A	ENSP00000390317.3:p.Ile1404Lys
ENST00000466382.2:c.780T>A
ENST00000636219.1:c.4217T>A	ENSP00000489842.1:p.Ile1406Lys
ENST00000637788.1:n.1163T>A
ENST00000324856.11:c.5363T>A	ENSP00000320485.7:p.Ile1788Lys
ENST00000374152.6:c.4214T>A	ENSP00000363267.2:p.Ile1405Lys
ENST00000430799.6:c.2052T>A
ENST00000457599.6:c.4712T>A	ENSP00000387636.2:p.Ile1571Lys
ENST00000466382.1:c.780T>A
ENST00000532781.1:c.861T>A
NM_006015.4:c.5363T>A , LRG_875t1:c.5363T>A	NP_006006.3:p.Ile1788Lys
NM_139135.2:c.4712T>A	NP_624361.1:p.Ile1571Lys
NM_006015.5:c.5363T>A	NP_006006.3:p.Ile1788Lys
NM_139135.3:c.4712T>A	NP_624361.1:p.Ile1571Lys
NM_006015.6:c.5363T>A MANE Select	NP_006006.3:p.Ile1788Lys
NM_139135.4:c.4712T>A	NP_624361.1:p.Ile1571Lys