Canonical Allele Identifier: CA279138

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 217291
• ClinVar RCV Id: RCV000201238 ; RCV002254285 ; RCV001221647
• dbSNP Id: rs863225060
• COSMIC: COSM163485 ; COSM1484857
• MyVariant Identifiers: chr3:g.178916924C>T (hg19) ; chr3:g.179199136C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179199136C>T , CM000665.2:g.179199136C>T	GRCh38
NC_000003.11:g.178916924C>T , CM000665.1:g.178916924C>T	GRCh37
NC_000003.10:g.180399618C>T	NCBI36
NG_012113.2:g.55614C>T , LRG_310:g.55614C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.311C>T MANE Select	ENSP00000263967.3:p.Pro104Leu
ENST00000643187.1:c.311C>T	ENSP00000493507.1:p.Pro104Leu
ENST00000675467.1:n.3118C>T
ENST00000675786.1:c.311C>T	ENSP00000502323.1:p.Pro104Leu
ENST00000263967.3:c.311C>T	ENSP00000263967.3:p.Pro104Leu
ENST00000468036.1:c.311C>T	ENSP00000417479.1:p.Pro104Leu
NM_006218.2:c.311C>T , LRG_310t1:c.311C>T	NP_006209.2:p.Pro104Leu
XM_006713658.2:c.311C>T	XP_006713721.1:p.Pro104Leu
XM_011512894.1:c.311C>T	XP_011511196.1:p.Pro104Leu
NM_006218.3:c.311C>T	NP_006209.2:p.Pro104Leu
XM_006713658.4:c.311C>T	XP_006713721.1:p.Pro104Leu
XM_011512894.2:c.311C>T	XP_011511196.1:p.Pro104Leu
NM_006218.4:c.311C>T MANE Select	NP_006209.2:p.Pro104Leu