Canonical Allele Identifier: CA355266131

Gene: PIK3CA

Linked Data

• MyVariant Identifiers: chr3:g.178937408T>C (hg19) ; chr3:g.179219620T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219620T>C , CM000665.2:g.179219620T>C	GRCh38
NC_000003.11:g.178937408T>C , CM000665.1:g.178937408T>C	GRCh37
NC_000003.10:g.180420102T>C	NCBI36
NG_012113.2:g.76098T>C , LRG_310:g.76098T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1796T>C MANE Select	ENSP00000263967.3:p.Met599Thr
ENST00000462255.2:n.258T>C
ENST00000643187.1:c.1796T>C	ENSP00000493507.1:p.Met599Thr
ENST00000674534.1:n.2704T>C
ENST00000674622.1:c.217T>C	ENSP00000502417.1:n.217T>C
ENST00000675467.1:n.4603T>C
ENST00000675786.1:c.*363T>C	ENSP00000502323.1:n.*363T>C
ENST00000263967.3:c.1796T>C	ENSP00000263967.3:p.Met599Thr
ENST00000462255.1:n.70T>C
NM_006218.2:c.1796T>C , LRG_310t1:c.1796T>C	NP_006209.2:p.Met599Thr
XM_006713658.2:c.1796T>C	XP_006713721.1:p.Met599Thr
XM_011512894.1:c.1796T>C	XP_011511196.1:p.Met599Thr
NM_006218.3:c.1796T>C	NP_006209.2:p.Met599Thr
XM_006713658.4:c.1796T>C	XP_006713721.1:p.Met599Thr
XM_011512894.2:c.1796T>C	XP_011511196.1:p.Met599Thr
NM_006218.4:c.1796T>C MANE Select	NP_006209.2:p.Met599Thr