Canonical Allele Identifier: CA2710803

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 246679
• ClinVar RCV Id: RCV000235538
• dbSNP Id: rs201779641
• ExAC: 3:178937350 C / T
• gnomAD v2: 3-178937350-C-T
• gnomAD v3: 3-179219562-C-T
• gnomAD v4: 3-179219562-C-T
• MyVariant Identifiers: chr3:g.178937350C>T (hg19) ; chr3:g.179219562C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219562C>T , CM000665.2:g.179219562C>T	GRCh38
NC_000003.11:g.178937350C>T , CM000665.1:g.178937350C>T	GRCh37
NC_000003.10:g.180420044C>T	NCBI36
NG_012113.2:g.76040C>T , LRG_310:g.76040C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.1747-9C>T MANE Select	ENSP00000263967.3:n.1747-9C>T
ENST00000462255.2:n.209-9C>T
ENST00000643187.1:c.1747-9C>T	ENSP00000493507.1:n.1747-9C>T
ENST00000674534.1:n.2646C>T
ENST00000674622.1:c.168-9C>T	ENSP00000502417.1:n.168-9C>T
ENST00000675467.1:n.4554-9C>T
ENST00000675786.1:c.*314-9C>T	ENSP00000502323.1:n.*314-9C>T
ENST00000263967.3:c.1747-9C>T	ENSP00000263967.3:n.1747-9C>T
ENST00000462255.1:n.12C>T
NM_006218.2:c.1747-9C>T , LRG_310t1:c.1747-9C>T	NP_006209.2:n.1747-9C>T
XM_006713658.2:c.1747-9C>T	XP_006713721.1:n.1747-9C>T
XM_011512894.1:c.1747-9C>T	XP_011511196.1:n.1747-9C>T
NM_006218.3:c.1747-9C>T	NP_006209.2:n.1747-9C>T
XM_006713658.4:c.1747-9C>T	XP_006713721.1:n.1747-9C>T
XM_011512894.2:c.1747-9C>T	XP_011511196.1:n.1747-9C>T
NM_006218.4:c.1747-9C>T MANE Select	NP_006209.2:n.1747-9C>T