Canonical Allele Identifier: CA355265245

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108408450
• gnomAD v4: 3-179218327-A-C
• MyVariant Identifiers: chr3:g.178936115A>C (hg19) ; chr3:g.179218327A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218327A>C , CM000665.2:g.179218327A>C	GRCh38
NC_000003.11:g.178936115A>C , CM000665.1:g.178936115A>C	GRCh37
NC_000003.10:g.180418809A>C	NCBI36
NG_012113.2:g.74805A>C , LRG_310:g.74805A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1657A>C MANE Select	ENSP00000263967.3:p.Ser553Arg
ENST00000462255.2:n.119A>C
ENST00000643187.1:c.1657A>C	ENSP00000493507.1:p.Ser553Arg
ENST00000674534.1:n.1411A>C
ENST00000674622.1:c.160A>C	ENSP00000502417.1:p.Ser54Arg
ENST00000675467.1:n.4464A>C
ENST00000675786.1:c.*224A>C	ENSP00000502323.1:n.*224A>C
ENST00000263967.3:c.1657A>C	ENSP00000263967.3:p.Ser553Arg
NM_006218.2:c.1657A>C , LRG_310t1:c.1657A>C	NP_006209.2:p.Ser553Arg
XM_006713658.2:c.1657A>C	XP_006713721.1:p.Ser553Arg
XM_011512894.1:c.1657A>C	XP_011511196.1:p.Ser553Arg
NM_006218.3:c.1657A>C	NP_006209.2:p.Ser553Arg
XM_006713658.4:c.1657A>C	XP_006713721.1:p.Ser553Arg
XM_011512894.2:c.1657A>C	XP_011511196.1:p.Ser553Arg
NM_006218.4:c.1657A>C MANE Select	NP_006209.2:p.Ser553Arg