Canonical Allele Identifier: CA339264586
Gene: ARID1A HGNC NCBI

Linked Data

dbSNP Id: rs1367702736

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26696590G>C , CM000663.2:g.26696590G>C GRCh38
NC_000001.10:g.27023081G>C , CM000663.1:g.27023081G>C GRCh37
NC_000001.9:g.26895668G>C NCBI36
NG_029965.1:g.5560G>C , LRG_875:g.5560G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324856.13:c.187G>C MANE Select ENSP00000320485.7:p.Val63Leu
ENST00000430799.7:c.-13+2973G>C ENSP00000390317.3:n.-13+2973G>C
ENST00000637465.1:c.-13+490G>C ENSP00000490650.1:n.-13+490G>C
ENST00000324856.11:c.187G>C ENSP00000320485.7:p.Val63Leu
ENST00000457599.6:c.187G>C ENSP00000387636.2:p.Val63Leu
NM_006015.4:c.187G>C , LRG_875t1:c.187G>C NP_006006.3:p.Val63Leu
NM_139135.2:c.187G>C NP_624361.1:p.Val63Leu
NM_006015.5:c.187G>C NP_006006.3:p.Val63Leu
NM_139135.3:c.187G>C NP_624361.1:p.Val63Leu
NM_006015.6:c.187G>C MANE Select NP_006006.3:p.Val63Leu
NM_139135.4:c.187G>C NP_624361.1:p.Val63Leu