Canonical Allele Identifier: CA355285844

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1057519932
• COSMIC: COSM1041524 ; COSM1041525
• MyVariant Identifiers: chr3:g.178952086T>A (hg19) ; chr3:g.179234298T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234298T>A , CM000665.2:g.179234298T>A	GRCh38
NC_000003.11:g.178952086T>A , CM000665.1:g.178952086T>A	GRCh37
NC_000003.10:g.180434780T>A	NCBI36
NG_012113.2:g.90776T>A , LRG_310:g.90776T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3141T>A MANE Select	ENSP00000263967.3:p.His1047Gln
ENST00000462255.2:n.2164T>A
ENST00000643187.1:c.*221T>A	ENSP00000493507.1:n.*221T>A
ENST00000674534.1:n.4049T>A
ENST00000674622.1:c.1562T>A	ENSP00000502417.1:n.1562T>A
ENST00000675467.1:n.5948T>A
ENST00000675786.1:c.*1708T>A	ENSP00000502323.1:n.*1708T>A
ENST00000675796.1:n.3036T>A
ENST00000263967.3:c.3141T>A	ENSP00000263967.3:p.His1047Gln
NM_006218.2:c.3141T>A , LRG_310t1:c.3141T>A	NP_006209.2:p.His1047Gln
XM_006713658.2:c.3141T>A	XP_006713721.1:p.His1047Gln
XM_011512894.1:c.3141T>A	XP_011511196.1:p.His1047Gln
NM_006218.3:c.3141T>A	NP_006209.2:p.His1047Gln
XM_006713658.4:c.3141T>A	XP_006713721.1:p.His1047Gln
XM_011512894.2:c.3141T>A	XP_011511196.1:p.His1047Gln
NM_006218.4:c.3141T>A MANE Select	NP_006209.2:p.His1047Gln