Canonical Allele Identifier: CA355285820

Gene: PIK3CA

Linked Data

• dbSNP Id: rs121913283
• COSMIC: COSM94984 ; COSM94985
• MyVariant Identifiers: chr3:g.178952074G>C (hg19) ; chr3:g.179234286G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234286G>C , CM000665.2:g.179234286G>C	GRCh38
NC_000003.11:g.178952074G>C , CM000665.1:g.178952074G>C	GRCh37
NC_000003.10:g.180434768G>C	NCBI36
NG_012113.2:g.90764G>C , LRG_310:g.90764G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3129G>C MANE Select	ENSP00000263967.3:p.Met1043Ile
ENST00000462255.2:n.2152G>C
ENST00000643187.1:c.*209G>C	ENSP00000493507.1:n.*209G>C
ENST00000674534.1:n.4037G>C
ENST00000674622.1:c.1550G>C	ENSP00000502417.1:n.1550G>C
ENST00000675467.1:n.5936G>C
ENST00000675786.1:c.*1696G>C	ENSP00000502323.1:n.*1696G>C
ENST00000675796.1:n.3024G>C
ENST00000263967.3:c.3129G>C	ENSP00000263967.3:p.Met1043Ile
NM_006218.2:c.3129G>C , LRG_310t1:c.3129G>C	NP_006209.2:p.Met1043Ile
XM_006713658.2:c.3129G>C	XP_006713721.1:p.Met1043Ile
XM_011512894.1:c.3129G>C	XP_011511196.1:p.Met1043Ile
NM_006218.3:c.3129G>C	NP_006209.2:p.Met1043Ile
XM_006713658.4:c.3129G>C	XP_006713721.1:p.Met1043Ile
XM_011512894.2:c.3129G>C	XP_011511196.1:p.Met1043Ile
NM_006218.4:c.3129G>C MANE Select	NP_006209.2:p.Met1043Ile