Canonical Allele Identifier: CA16602379

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 375896
• ClinVar RCV Id: RCV000418587 ; RCV000418767 ; RCV000421622 ; RCV000422954 ; RCV000423574 ; RCV000423978 ; RCV000424431 ; RCV000425714 ; RCV000427263 ; RCV000429497 ; RCV000430168 ; RCV000431018 ; RCV000431401 ; RCV000434277 ; RCV000434629 ; RCV000435117 ; RCV000435310 ; RCV000435795 ; RCV000436433 ; RCV000440189 ; RCV000441730 ; RCV000442112 ; RCV000442200 ; RCV000442485 ; RCV000443141 ; RCV000445019 ; RCV000626447
• dbSNP Id: rs104886003
• COSMIC: COSM27133 ; COSM295672
• MyVariant Identifiers: chr3:g.178936091G>C (hg19) ; chr3:g.179218303G>C (hg38)
• CIViC: CA16602379
• PubMed: PMID:15016963 ; PMID:15254419 ; PMID:15647370 ; PMID:15805248 ; PMID:16906227 ; PMID:18676830 ; PMID:18725974 ; PMID:19029981 ; PMID:19366826 ; PMID:19513541 ; PMID:19903786 ; PMID:20453058 ; PMID:20619739 ; PMID:21430269 ; PMID:22162582 ; PMID:22162589 ; PMID:23408298 ; PMID:25157968 ; PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218303G>C , CM000665.2:g.179218303G>C	GRCh38
NC_000003.11:g.178936091G>C , CM000665.1:g.178936091G>C	GRCh37
NC_000003.10:g.180418785G>C	NCBI36
NG_012113.2:g.74781G>C , LRG_310:g.74781G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.1633G>C MANE Select	ENSP00000263967.3:p.Glu545Gln
ENST00000462255.2:n.95G>C
ENST00000643187.1:c.1633G>C	ENSP00000493507.1:p.Glu545Gln
ENST00000674534.1:n.1387G>C
ENST00000674622.1:c.136G>C	ENSP00000502417.1:p.Glu46Gln
ENST00000675467.1:n.4440G>C
ENST00000675786.1:c.*200G>C	ENSP00000502323.1:n.*200G>C
ENST00000263967.3:c.1633G>C	ENSP00000263967.3:p.Glu545Gln
NM_006218.2:c.1633G>C , LRG_310t1:c.1633G>C	NP_006209.2:p.Glu545Gln
XM_006713658.2:c.1633G>C	XP_006713721.1:p.Glu545Gln
XM_011512894.1:c.1633G>C	XP_011511196.1:p.Glu545Gln
NM_006218.3:c.1633G>C	NP_006209.2:p.Glu545Gln
XM_006713658.4:c.1633G>C	XP_006713721.1:p.Glu545Gln
XM_011512894.2:c.1633G>C	XP_011511196.1:p.Glu545Gln
NM_006218.4:c.1633G>C MANE Select	NP_006209.2:p.Glu545Gln