Canonical Allele Identifier: CA355279602

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1227389466
• gnomAD v2: 3-178921336-T-C
• gnomAD v4: 3-179203548-T-C
• MyVariant Identifiers: chr3:g.178921336T>C (hg19) ; chr3:g.179203548T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203548T>C , CM000665.2:g.179203548T>C	GRCh38
NC_000003.11:g.178921336T>C , CM000665.1:g.178921336T>C	GRCh37
NC_000003.10:g.180404030T>C	NCBI36
NG_012113.2:g.60026T>C , LRG_310:g.60026T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.818T>C MANE Select	ENSP00000263967.3:p.Ile273Thr
ENST00000643187.1:c.818T>C	ENSP00000493507.1:p.Ile273Thr
ENST00000674534.1:n.572T>C
ENST00000675467.1:n.3625T>C
ENST00000675786.1:c.818T>C	ENSP00000502323.1:p.Ile273Thr
ENST00000263967.3:c.818T>C	ENSP00000263967.3:p.Ile273Thr
NM_006218.2:c.818T>C , LRG_310t1:c.818T>C	NP_006209.2:p.Ile273Thr
XM_006713658.2:c.818T>C	XP_006713721.1:p.Ile273Thr
XM_011512894.1:c.818T>C	XP_011511196.1:p.Ile273Thr
NM_006218.3:c.818T>C	NP_006209.2:p.Ile273Thr
XM_006713658.4:c.818T>C	XP_006713721.1:p.Ile273Thr
XM_011512894.2:c.818T>C	XP_011511196.1:p.Ile273Thr
NM_006218.4:c.818T>C MANE Select	NP_006209.2:p.Ile273Thr