Canonical Allele Identifier: CA437038189

Gene: PIK3CA

Linked Data

• MyVariant Identifiers: chr3:g.178947894G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179230106G>C , CM000665.2:g.179230106G>C	GRCh38
NC_000003.11:g.178947894G>C , CM000665.1:g.178947894G>C	GRCh37
NC_000003.10:g.180430588G>C	NCBI36
NG_012113.2:g.86584G>C , LRG_310:g.86584G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.2769G>C MANE Select	ENSP00000263967.3:p.Val923=
ENST00000462255.2:n.1792G>C
ENST00000643187.1:c.2769G>C	ENSP00000493507.1:p.Val923=
ENST00000674534.1:n.3677G>C
ENST00000674622.1:c.1190G>C	ENSP00000502417.1:n.1190G>C
ENST00000675467.1:n.5576G>C
ENST00000675786.1:c.*1336G>C	ENSP00000502323.1:n.*1336G>C
ENST00000675796.1:n.2664G>C
ENST00000263967.3:c.2769G>C	ENSP00000263967.3:p.Val923=
NM_006218.2:c.2769G>C , LRG_310t1:c.2769G>C	NP_006209.2:p.Val923=
XM_006713658.2:c.2769G>C	XP_006713721.1:p.Val923=
XM_011512894.1:c.2769G>C	XP_011511196.1:p.Val923=
NM_006218.3:c.2769G>C	NP_006209.2:p.Val923=
XM_006713658.4:c.2769G>C	XP_006713721.1:p.Val923=
XM_011512894.2:c.2769G>C	XP_011511196.1:p.Val923=
NM_006218.4:c.2769G>C MANE Select	NP_006209.2:p.Val923=