Canonical Allele Identifier: CA355281700

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1006152
• ClinVar RCV Id: RCV001303149
• dbSNP Id: rs1724484731
• MyVariant Identifiers: chr3:g.178921573A>T (hg19) ; chr3:g.179203785A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203785A>T , CM000665.2:g.179203785A>T	GRCh38
NC_000003.11:g.178921573A>T , CM000665.1:g.178921573A>T	GRCh37
NC_000003.10:g.180404267A>T	NCBI36
NG_012113.2:g.60263A>T , LRG_310:g.60263A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1055A>T MANE Select	ENSP00000263967.3:p.Asp352Val
ENST00000643187.1:c.1055A>T	ENSP00000493507.1:p.Asp352Val
ENST00000674534.1:n.809A>T
ENST00000675467.1:n.3862A>T
ENST00000675786.1:c.1055A>T	ENSP00000502323.1:p.Asp352Val
ENST00000263967.3:c.1055A>T	ENSP00000263967.3:p.Asp352Val
NM_006218.2:c.1055A>T , LRG_310t1:c.1055A>T	NP_006209.2:p.Asp352Val
XM_006713658.2:c.1055A>T	XP_006713721.1:p.Asp352Val
XM_011512894.1:c.1055A>T	XP_011511196.1:p.Asp352Val
NM_006218.3:c.1055A>T	NP_006209.2:p.Asp352Val
XM_006713658.4:c.1055A>T	XP_006713721.1:p.Asp352Val
XM_011512894.2:c.1055A>T	XP_011511196.1:p.Asp352Val
NM_006218.4:c.1055A>T MANE Select	NP_006209.2:p.Asp352Val