Canonical Allele Identifier: CA1160180548
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs2080252698

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696390A>C , CM000663.2:g.26696390A>C GRCh38
NC_000001.10:g.27022881A>C , CM000663.1:g.27022881A>C GRCh37
NC_000001.9:g.26895468A>C NCBI36
NG_029965.1:g.5360A>C , LRG_875:g.5360A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.-14A>C MANE Select ENSP00000320485.7:n.-14A>C
ENST00000430799.7:c.-13+2773A>C ENSP00000390317.3:n.-13+2773A>C
ENST00000637465.1:c.-13+290A>C ENSP00000490650.1:n.-13+290A>C
ENST00000324856.11:c.-14A>C ENSP00000320485.7:n.-14A>C
NM_006015.4:c.-14A>C , LRG_875t1:c.-14A>C NP_006006.3:n.-14A>C
NM_139135.2:c.-14A>C NP_624361.1:n.-14A>C
XM_011542542.1:c.16T>G XP_011540844.1:p.Ser6Ala
NM_006015.5:c.-14A>C NP_006006.3:n.-14A>C
NM_139135.3:c.-14A>C NP_624361.1:n.-14A>C
NM_006015.6:c.-14A>C MANE Select NP_006006.3:n.-14A>C
NM_139135.4:c.-14A>C NP_624361.1:n.-14A>C