Canonical Allele Identifier: CA355280519

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 2096884
• ClinVar RCV Id: RCV003028325
• dbSNP Id: rs2108392942
• MyVariant Identifiers: chr3:g.178921450T>C (hg19) ; chr3:g.179203662T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203662T>C , CM000665.2:g.179203662T>C	GRCh38
NC_000003.11:g.178921450T>C , CM000665.1:g.178921450T>C	GRCh37
NC_000003.10:g.180404144T>C	NCBI36
NG_012113.2:g.60140T>C , LRG_310:g.60140T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.932T>C MANE Select	ENSP00000263967.3:p.Ile311Thr
ENST00000643187.1:c.932T>C	ENSP00000493507.1:p.Ile311Thr
ENST00000674534.1:n.686T>C
ENST00000675467.1:n.3739T>C
ENST00000675786.1:c.932T>C	ENSP00000502323.1:p.Ile311Thr
ENST00000263967.3:c.932T>C	ENSP00000263967.3:p.Ile311Thr
NM_006218.2:c.932T>C , LRG_310t1:c.932T>C	NP_006209.2:p.Ile311Thr
XM_006713658.2:c.932T>C	XP_006713721.1:p.Ile311Thr
XM_011512894.1:c.932T>C	XP_011511196.1:p.Ile311Thr
NM_006218.3:c.932T>C	NP_006209.2:p.Ile311Thr
XM_006713658.4:c.932T>C	XP_006713721.1:p.Ile311Thr
XM_011512894.2:c.932T>C	XP_011511196.1:p.Ile311Thr
NM_006218.4:c.932T>C MANE Select	NP_006209.2:p.Ile311Thr