Canonical Allele Identifier: CA16602927

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 376495
• ClinVar RCV Id: RCV000425565 ; RCV000426273 ; RCV000432150 ; RCV000432808 ; RCV000442897 ; RCV000442990
• dbSNP Id: rs772110575
• COSMIC: COSM729833 ; COSM729834
• MyVariant Identifiers: chr3:g.178916726G>T (hg19) ; chr3:g.179198938G>T (hg38)
• PubMed: PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179198938G>T , CM000665.2:g.179198938G>T	GRCh38
NC_000003.11:g.178916726G>T , CM000665.1:g.178916726G>T	GRCh37
NC_000003.10:g.180399420G>T	NCBI36
NG_012113.2:g.55416G>T , LRG_310:g.55416G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.113G>T MANE Select	ENSP00000263967.3:p.Arg38Leu
ENST00000643187.1:c.113G>T	ENSP00000493507.1:p.Arg38Leu
ENST00000675467.1:n.2920G>T
ENST00000675786.1:c.113G>T	ENSP00000502323.1:p.Arg38Leu
ENST00000263967.3:c.113G>T	ENSP00000263967.3:p.Arg38Leu
ENST00000468036.1:c.113G>T	ENSP00000417479.1:p.Arg38Leu
NM_006218.2:c.113G>T , LRG_310t1:c.113G>T	NP_006209.2:p.Arg38Leu
XM_006713658.2:c.113G>T	XP_006713721.1:p.Arg38Leu
XM_011512894.1:c.113G>T	XP_011511196.1:p.Arg38Leu
NM_006218.3:c.113G>T	NP_006209.2:p.Arg38Leu
XM_006713658.4:c.113G>T	XP_006713721.1:p.Arg38Leu
XM_011512894.2:c.113G>T	XP_011511196.1:p.Arg38Leu
NM_006218.4:c.113G>T MANE Select	NP_006209.2:p.Arg38Leu