Canonical Allele Identifier: CA339184909

Gene: ARID1A

Linked Data

• MyVariant Identifiers: chr1:g.27105740A>C (hg19) ; chr1:g.26779249A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779249A>C , CM000663.2:g.26779249A>C	GRCh38
NC_000001.10:g.27105740A>C , CM000663.1:g.27105740A>C	GRCh37
NC_000001.9:g.26978327A>C	NCBI36
NG_029965.1:g.88219A>C , LRG_875:g.88219A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324856.13:c.5351A>C MANE Select	ENSP00000320485.7:p.Asn1784Thr
ENST00000374152.7:c.4202A>C	ENSP00000363267.2:p.Asn1401Thr
ENST00000430799.7:c.4199A>C	ENSP00000390317.3:p.Asn1400Thr
ENST00000466382.2:c.768A>C
ENST00000636219.1:c.4205A>C	ENSP00000489842.1:p.Asn1402Thr
ENST00000637788.1:n.1151A>C
ENST00000324856.11:c.5351A>C	ENSP00000320485.7:p.Asn1784Thr
ENST00000374152.6:c.4202A>C	ENSP00000363267.2:p.Asn1401Thr
ENST00000430799.6:c.2040A>C
ENST00000457599.6:c.4700A>C	ENSP00000387636.2:p.Asn1567Thr
ENST00000466382.1:c.768A>C
ENST00000532781.1:c.849A>C
NM_006015.4:c.5351A>C , LRG_875t1:c.5351A>C	NP_006006.3:p.Asn1784Thr
NM_139135.2:c.4700A>C	NP_624361.1:p.Asn1567Thr
NM_006015.5:c.5351A>C	NP_006006.3:p.Asn1784Thr
NM_139135.3:c.4700A>C	NP_624361.1:p.Asn1567Thr
NM_006015.6:c.5351A>C MANE Select	NP_006006.3:p.Asn1784Thr
NM_139135.4:c.4700A>C	NP_624361.1:p.Asn1567Thr