Canonical Allele Identifier: CA339184552
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs2081165896

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26779182G>T , CM000663.2:g.26779182G>T GRCh38
NC_000001.10:g.27105673G>T , CM000663.1:g.27105673G>T GRCh37
NC_000001.9:g.26978260G>T NCBI36
NG_029965.1:g.88152G>T , LRG_875:g.88152G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.5284G>T MANE Select ENSP00000320485.7:p.Gly1762Trp
ENST00000374152.7:c.4135G>T ENSP00000363267.2:p.Gly1379Trp
ENST00000430799.7:c.4132G>T ENSP00000390317.3:p.Gly1378Trp
ENST00000466382.2:c.701G>T
ENST00000636219.1:c.4138G>T ENSP00000489842.1:p.Gly1380Trp
ENST00000637788.1:n.1084G>T
ENST00000324856.11:c.5284G>T ENSP00000320485.7:p.Gly1762Trp
ENST00000374152.6:c.4135G>T ENSP00000363267.2:p.Gly1379Trp
ENST00000430799.6:c.1973G>T
ENST00000457599.6:c.4633G>T ENSP00000387636.2:p.Gly1545Trp
ENST00000466382.1:c.701G>T
ENST00000532781.1:c.782G>T
NM_006015.4:c.5284G>T , LRG_875t1:c.5284G>T NP_006006.3:p.Gly1762Trp
NM_139135.2:c.4633G>T NP_624361.1:p.Gly1545Trp
NM_006015.5:c.5284G>T NP_006006.3:p.Gly1762Trp
NM_139135.3:c.4633G>T NP_624361.1:p.Gly1545Trp
NM_006015.6:c.5284G>T MANE Select NP_006006.3:p.Gly1762Trp
NM_139135.4:c.4633G>T NP_624361.1:p.Gly1545Trp