Canonical Allele Identifier: CA339184455
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs759947795

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26779158T>G , CM000663.2:g.26779158T>G GRCh38
NC_000001.10:g.27105649T>G , CM000663.1:g.27105649T>G GRCh37
NC_000001.9:g.26978236T>G NCBI36
NG_029965.1:g.88128T>G , LRG_875:g.88128T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000324856.13:c.5260T>G MANE Select ENSP00000320485.7:p.Ser1754Ala
ENST00000374152.7:c.4111T>G ENSP00000363267.2:p.Ser1371Ala
ENST00000430799.7:c.4108T>G ENSP00000390317.3:p.Ser1370Ala
ENST00000466382.2:c.677T>G
ENST00000636219.1:c.4114T>G ENSP00000489842.1:p.Ser1372Ala
ENST00000637788.1:n.1060T>G
ENST00000324856.11:c.5260T>G ENSP00000320485.7:p.Ser1754Ala
ENST00000374152.6:c.4111T>G ENSP00000363267.2:p.Ser1371Ala
ENST00000430799.6:c.1949T>G
ENST00000457599.6:c.4609T>G ENSP00000387636.2:p.Ser1537Ala
ENST00000466382.1:c.677T>G
ENST00000532781.1:c.758T>G
NM_006015.4:c.5260T>G , LRG_875t1:c.5260T>G NP_006006.3:p.Ser1754Ala
NM_139135.2:c.4609T>G NP_624361.1:p.Ser1537Ala
NM_006015.5:c.5260T>G NP_006006.3:p.Ser1754Ala
NM_139135.3:c.4609T>G NP_624361.1:p.Ser1537Ala
NM_006015.6:c.5260T>G MANE Select NP_006006.3:p.Ser1754Ala
NM_139135.4:c.4609T>G NP_624361.1:p.Ser1537Ala