Canonical Allele Identifier: CA416968020

Gene: ARID1A

Linked Data

• MyVariant Identifiers: chr1:g.27105651T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779160T>C , CM000663.2:g.26779160T>C	GRCh38
NC_000001.10:g.27105651T>C , CM000663.1:g.27105651T>C	GRCh37
NC_000001.9:g.26978238T>C	NCBI36
NG_029965.1:g.88130T>C , LRG_875:g.88130T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5262T>C MANE Select	ENSP00000320485.7:p.Ser1754=
ENST00000374152.7:c.4113T>C	ENSP00000363267.2:p.Ser1371=
ENST00000430799.7:c.4110T>C	ENSP00000390317.3:p.Ser1370=
ENST00000466382.2:c.679T>C
ENST00000636219.1:c.4116T>C	ENSP00000489842.1:p.Ser1372=
ENST00000637788.1:n.1062T>C
ENST00000324856.11:c.5262T>C	ENSP00000320485.7:p.Ser1754=
ENST00000374152.6:c.4113T>C	ENSP00000363267.2:p.Ser1371=
ENST00000430799.6:c.1951T>C
ENST00000457599.6:c.4611T>C	ENSP00000387636.2:p.Ser1537=
ENST00000466382.1:c.679T>C
ENST00000532781.1:c.760T>C
NM_006015.4:c.5262T>C , LRG_875t1:c.5262T>C	NP_006006.3:p.Ser1754=
NM_139135.2:c.4611T>C	NP_624361.1:p.Ser1537=
NM_006015.5:c.5262T>C	NP_006006.3:p.Ser1754=
NM_139135.3:c.4611T>C	NP_624361.1:p.Ser1537=
NM_006015.6:c.5262T>C MANE Select	NP_006006.3:p.Ser1754=
NM_139135.4:c.4611T>C	NP_624361.1:p.Ser1537=