Canonical Allele Identifier: CA355284931

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 2069684
• ClinVar RCV Id: RCV002962367
• dbSNP Id: rs2108429272
• COSMIC: COSM21446 ; COSM1041516
• MyVariant Identifiers: chr3:g.178951957G>T (hg19) ; chr3:g.179234169G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234169G>T , CM000665.2:g.179234169G>T	GRCh38
NC_000003.11:g.178951957G>T , CM000665.1:g.178951957G>T	GRCh37
NC_000003.10:g.180434651G>T	NCBI36
NG_012113.2:g.90647G>T , LRG_310:g.90647G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3012G>T MANE Select	ENSP00000263967.3:p.Met1004Ile
ENST00000462255.2:n.2035G>T
ENST00000643187.1:c.*92G>T	ENSP00000493507.1:n.*92G>T
ENST00000674534.1:n.3920G>T
ENST00000674622.1:c.1433G>T	ENSP00000502417.1:n.1433G>T
ENST00000675467.1:n.5819G>T
ENST00000675786.1:c.*1579G>T	ENSP00000502323.1:n.*1579G>T
ENST00000675796.1:n.2907G>T
ENST00000263967.3:c.3012G>T	ENSP00000263967.3:p.Met1004Ile
NM_006218.2:c.3012G>T , LRG_310t1:c.3012G>T	NP_006209.2:p.Met1004Ile
XM_006713658.2:c.3012G>T	XP_006713721.1:p.Met1004Ile
XM_011512894.1:c.3012G>T	XP_011511196.1:p.Met1004Ile
NM_006218.3:c.3012G>T	NP_006209.2:p.Met1004Ile
XM_006713658.4:c.3012G>T	XP_006713721.1:p.Met1004Ile
XM_011512894.2:c.3012G>T	XP_011511196.1:p.Met1004Ile
NM_006218.4:c.3012G>T MANE Select	NP_006209.2:p.Met1004Ile