Canonical Allele Identifier: CA355266034

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 3225339
• ClinVar RCV Id: RCV004523987
• dbSNP Id: rs2108410741
• MyVariant Identifiers: chr3:g.178937396C>T (hg19) ; chr3:g.179219608C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219608C>T , CM000665.2:g.179219608C>T	GRCh38
NC_000003.11:g.178937396C>T , CM000665.1:g.178937396C>T	GRCh37
NC_000003.10:g.180420090C>T	NCBI36
NG_012113.2:g.76086C>T , LRG_310:g.76086C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1784C>T MANE Select	ENSP00000263967.3:p.Pro595Leu
ENST00000462255.2:n.246C>T
ENST00000643187.1:c.1784C>T	ENSP00000493507.1:p.Pro595Leu
ENST00000674534.1:n.2692C>T
ENST00000674622.1:c.205C>T	ENSP00000502417.1:n.205C>T
ENST00000675467.1:n.4591C>T
ENST00000675786.1:c.*351C>T	ENSP00000502323.1:n.*351C>T
ENST00000263967.3:c.1784C>T	ENSP00000263967.3:p.Pro595Leu
ENST00000462255.1:n.58C>T
NM_006218.2:c.1784C>T , LRG_310t1:c.1784C>T	NP_006209.2:p.Pro595Leu
XM_006713658.2:c.1784C>T	XP_006713721.1:p.Pro595Leu
XM_011512894.1:c.1784C>T	XP_011511196.1:p.Pro595Leu
NM_006218.3:c.1784C>T	NP_006209.2:p.Pro595Leu
XM_006713658.4:c.1784C>T	XP_006713721.1:p.Pro595Leu
XM_011512894.2:c.1784C>T	XP_011511196.1:p.Pro595Leu
NM_006218.4:c.1784C>T MANE Select	NP_006209.2:p.Pro595Leu