Canonical Allele Identifier: CA339184718

Gene: ARID1A

Linked Data

• dbSNP Id: rs2124138118
• COSMIC: COSM4431049
• MyVariant Identifiers: chr1:g.27105705A>T (hg19) ; chr1:g.26779214A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779214A>T , CM000663.2:g.26779214A>T	GRCh38
NC_000001.10:g.27105705A>T , CM000663.1:g.27105705A>T	GRCh37
NC_000001.9:g.26978292A>T	NCBI36
NG_029965.1:g.88184A>T , LRG_875:g.88184A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5316A>T MANE Select	ENSP00000320485.7:p.Lys1772Asn
ENST00000374152.7:c.4167A>T	ENSP00000363267.2:p.Lys1389Asn
ENST00000430799.7:c.4164A>T	ENSP00000390317.3:p.Lys1388Asn
ENST00000466382.2:c.733A>T
ENST00000636219.1:c.4170A>T	ENSP00000489842.1:p.Lys1390Asn
ENST00000637788.1:n.1116A>T
ENST00000324856.11:c.5316A>T	ENSP00000320485.7:p.Lys1772Asn
ENST00000374152.6:c.4167A>T	ENSP00000363267.2:p.Lys1389Asn
ENST00000430799.6:c.2005A>T
ENST00000457599.6:c.4665A>T	ENSP00000387636.2:p.Lys1555Asn
ENST00000466382.1:c.733A>T
ENST00000532781.1:c.814A>T
NM_006015.4:c.5316A>T , LRG_875t1:c.5316A>T	NP_006006.3:p.Lys1772Asn
NM_139135.2:c.4665A>T	NP_624361.1:p.Lys1555Asn
NM_006015.5:c.5316A>T	NP_006006.3:p.Lys1772Asn
NM_139135.3:c.4665A>T	NP_624361.1:p.Lys1555Asn
NM_006015.6:c.5316A>T MANE Select	NP_006006.3:p.Lys1772Asn
NM_139135.4:c.4665A>T	NP_624361.1:p.Lys1555Asn