Canonical Allele Identifier: CA437032893

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1121967
• ClinVar RCV Id: RCV001452427 ; RCV002405065
• dbSNP Id: rs2108408180
• MyVariant Identifiers: chr3:g.178936060T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218272T>C , CM000665.2:g.179218272T>C	GRCh38
NC_000003.11:g.178936060T>C , CM000665.1:g.178936060T>C	GRCh37
NC_000003.10:g.180418754T>C	NCBI36
NG_012113.2:g.74750T>C , LRG_310:g.74750T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1602T>C MANE Select	ENSP00000263967.3:p.Ile534=
ENST00000462255.2:n.64T>C
ENST00000643187.1:c.1602T>C	ENSP00000493507.1:p.Ile534=
ENST00000674534.1:n.1356T>C
ENST00000674622.1:c.105T>C	ENSP00000502417.1:p.Ile35=
ENST00000675467.1:n.4409T>C
ENST00000675786.1:c.*169T>C	ENSP00000502323.1:n.*169T>C
ENST00000263967.3:c.1602T>C	ENSP00000263967.3:p.Ile534=
NM_006218.2:c.1602T>C , LRG_310t1:c.1602T>C	NP_006209.2:p.Ile534=
XM_006713658.2:c.1602T>C	XP_006713721.1:p.Ile534=
XM_011512894.1:c.1602T>C	XP_011511196.1:p.Ile534=
NM_006218.3:c.1602T>C	NP_006209.2:p.Ile534=
XM_006713658.4:c.1602T>C	XP_006713721.1:p.Ile534=
XM_011512894.2:c.1602T>C	XP_011511196.1:p.Ile534=
NM_006218.4:c.1602T>C MANE Select	NP_006209.2:p.Ile534=