Canonical Allele Identifier: CA11388442

Gene: PIK3CA

Linked Data

• dbSNP Id: rs870995
• gnomAD v2: 3-178913006-C-A
• gnomAD v3: 3-179195218-C-A
• gnomAD v4: 3-179195218-C-A
• MyVariant Identifiers: chr3:g.178913006C>A (hg19) ; chr3:g.179195218C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179195218C>A , CM000665.2:g.179195218C>A	GRCh38
NC_000003.11:g.178913006C>A , CM000665.1:g.178913006C>A	GRCh37
NC_000003.10:g.180395700C>A	NCBI36
NG_012113.2:g.51696C>A , LRG_310:g.51696C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.-76-3532C>A MANE Select	ENSP00000263967.3:n.-76-3532C>A
ENST00000643187.1:c.-76-3532C>A	ENSP00000493507.1:n.-76-3532C>A
ENST00000675786.1:c.-76-3532C>A	ENSP00000502323.1:n.-76-3532C>A
ENST00000263967.3:c.-76-3532C>A	ENSP00000263967.3:n.-76-3532C>A
ENST00000468036.1:c.-76-3532C>A	ENSP00000417479.1:n.-76-3532C>A
ENST00000477735.1:c.-76-3532C>A	ENSP00000418145.1:n.-76-3532C>A
NM_006218.2:c.-76-3532C>A , LRG_310t1:c.-76-3532C>A	NP_006209.2:n.-76-3532C>A
XM_006713658.2:c.-76-3532C>A	XP_006713721.1:n.-76-3532C>A
XM_011512894.1:c.-76-3532C>A	XP_011511196.1:n.-76-3532C>A
NM_006218.3:c.-76-3532C>A	NP_006209.2:n.-76-3532C>A
XM_006713658.4:c.-76-3532C>A	XP_006713721.1:n.-76-3532C>A
XM_011512894.2:c.-76-3532C>A	XP_011511196.1:n.-76-3532C>A
NM_006218.4:c.-76-3532C>A MANE Select	NP_006209.2:n.-76-3532C>A