Canonical Allele Identifier: CA355272520

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108386129
• MyVariant Identifiers: chr3:g.178916899C>G (hg19) ; chr3:g.179199111C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179199111C>G , CM000665.2:g.179199111C>G	GRCh38
NC_000003.11:g.178916899C>G , CM000665.1:g.178916899C>G	GRCh37
NC_000003.10:g.180399593C>G	NCBI36
NG_012113.2:g.55589C>G , LRG_310:g.55589C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.286C>G MANE Select	ENSP00000263967.3:p.Gln96Glu
ENST00000643187.1:c.286C>G	ENSP00000493507.1:p.Gln96Glu
ENST00000675467.1:n.3093C>G
ENST00000675786.1:c.286C>G	ENSP00000502323.1:p.Gln96Glu
ENST00000263967.3:c.286C>G	ENSP00000263967.3:p.Gln96Glu
ENST00000468036.1:c.286C>G	ENSP00000417479.1:p.Gln96Glu
NM_006218.2:c.286C>G , LRG_310t1:c.286C>G	NP_006209.2:p.Gln96Glu
XM_006713658.2:c.286C>G	XP_006713721.1:p.Gln96Glu
XM_011512894.1:c.286C>G	XP_011511196.1:p.Gln96Glu
NM_006218.3:c.286C>G	NP_006209.2:p.Gln96Glu
XM_006713658.4:c.286C>G	XP_006713721.1:p.Gln96Glu
XM_011512894.2:c.286C>G	XP_011511196.1:p.Gln96Glu
NM_006218.4:c.286C>G MANE Select	NP_006209.2:p.Gln96Glu