Canonical Allele Identifier: CA437038987

Gene: PIK3CA

Linked Data

• MyVariant Identifiers: chr3:g.178952101A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234313A>C , CM000665.2:g.179234313A>C	GRCh38
NC_000003.11:g.178952101A>C , CM000665.1:g.178952101A>C	GRCh37
NC_000003.10:g.180434795A>C	NCBI36
NG_012113.2:g.90791A>C , LRG_310:g.90791A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3156A>C MANE Select	ENSP00000263967.3:p.Thr1052=
ENST00000462255.2:n.2179A>C
ENST00000643187.1:c.*236A>C	ENSP00000493507.1:n.*236A>C
ENST00000674534.1:n.4064A>C
ENST00000674622.1:c.1577A>C	ENSP00000502417.1:n.1577A>C
ENST00000675467.1:n.5963A>C
ENST00000675786.1:c.*1723A>C	ENSP00000502323.1:n.*1723A>C
ENST00000675796.1:n.3051A>C
ENST00000263967.3:c.3156A>C	ENSP00000263967.3:p.Thr1052=
NM_006218.2:c.3156A>C , LRG_310t1:c.3156A>C	NP_006209.2:p.Thr1052=
XM_006713658.2:c.3156A>C	XP_006713721.1:p.Thr1052=
XM_011512894.1:c.3156A>C	XP_011511196.1:p.Thr1052=
NM_006218.3:c.3156A>C	NP_006209.2:p.Thr1052=
XM_006713658.4:c.3156A>C	XP_006713721.1:p.Thr1052=
XM_011512894.2:c.3156A>C	XP_011511196.1:p.Thr1052=
NM_006218.4:c.3156A>C MANE Select	NP_006209.2:p.Thr1052=