Canonical Allele Identifier: CA437033162

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108410956
• MyVariant Identifiers: chr3:g.178937448A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219660A>G , CM000665.2:g.179219660A>G	GRCh38
NC_000003.11:g.178937448A>G , CM000665.1:g.178937448A>G	GRCh37
NC_000003.10:g.180420142A>G	NCBI36
NG_012113.2:g.76138A>G , LRG_310:g.76138A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1836A>G MANE Select	ENSP00000263967.3:p.Arg612=
ENST00000462255.2:n.298A>G
ENST00000643187.1:c.1836A>G	ENSP00000493507.1:p.Arg612=
ENST00000674534.1:n.2744A>G
ENST00000674622.1:c.257A>G	ENSP00000502417.1:n.257A>G
ENST00000675467.1:n.4643A>G
ENST00000675786.1:c.*403A>G	ENSP00000502323.1:n.*403A>G
ENST00000263967.3:c.1836A>G	ENSP00000263967.3:p.Arg612=
ENST00000462255.1:n.110A>G
NM_006218.2:c.1836A>G , LRG_310t1:c.1836A>G	NP_006209.2:p.Arg612=
XM_006713658.2:c.1836A>G	XP_006713721.1:p.Arg612=
XM_011512894.1:c.1836A>G	XP_011511196.1:p.Arg612=
NM_006218.3:c.1836A>G	NP_006209.2:p.Arg612=
XM_006713658.4:c.1836A>G	XP_006713721.1:p.Arg612=
XM_011512894.2:c.1836A>G	XP_011511196.1:p.Arg612=
NM_006218.4:c.1836A>G MANE Select	NP_006209.2:p.Arg612=