Canonical Allele Identifier: CA339184508

Gene: ARID1A

Linked Data

• MyVariant Identifiers: chr1:g.27105665T>C (hg19) ; chr1:g.26779174T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779174T>C , CM000663.2:g.26779174T>C	GRCh38
NC_000001.10:g.27105665T>C , CM000663.1:g.27105665T>C	GRCh37
NC_000001.9:g.26978252T>C	NCBI36
NG_029965.1:g.88144T>C , LRG_875:g.88144T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5276T>C MANE Select	ENSP00000320485.7:p.Met1759Thr
ENST00000374152.7:c.4127T>C	ENSP00000363267.2:p.Met1376Thr
ENST00000430799.7:c.4124T>C	ENSP00000390317.3:p.Met1375Thr
ENST00000466382.2:c.693T>C
ENST00000636219.1:c.4130T>C	ENSP00000489842.1:p.Met1377Thr
ENST00000637788.1:n.1076T>C
ENST00000324856.11:c.5276T>C	ENSP00000320485.7:p.Met1759Thr
ENST00000374152.6:c.4127T>C	ENSP00000363267.2:p.Met1376Thr
ENST00000430799.6:c.1965T>C
ENST00000457599.6:c.4625T>C	ENSP00000387636.2:p.Met1542Thr
ENST00000466382.1:c.693T>C
ENST00000532781.1:c.774T>C
NM_006015.4:c.5276T>C , LRG_875t1:c.5276T>C	NP_006006.3:p.Met1759Thr
NM_139135.2:c.4625T>C	NP_624361.1:p.Met1542Thr
NM_006015.5:c.5276T>C	NP_006006.3:p.Met1759Thr
NM_139135.3:c.4625T>C	NP_624361.1:p.Met1542Thr
NM_006015.6:c.5276T>C MANE Select	NP_006006.3:p.Met1759Thr
NM_139135.4:c.4625T>C	NP_624361.1:p.Met1542Thr