Canonical Allele Identifier: CA11517671

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1228928
• ClinVar RCV Id: RCV001616559
• dbSNP Id: rs7623154
• gnomAD v2: 3-178921158-G-A
• gnomAD v3: 3-179203370-G-A
• gnomAD v4: 3-179203370-G-A
• MyVariant Identifiers: chr3:g.178921158G>A (hg19) ; chr3:g.179203370G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203370G>A , CM000665.2:g.179203370G>A	GRCh38
NC_000003.11:g.178921158G>A , CM000665.1:g.178921158G>A	GRCh37
NC_000003.10:g.180403852G>A	NCBI36
NG_012113.2:g.59848G>A , LRG_310:g.59848G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.814-174G>A MANE Select	ENSP00000263967.3:n.814-174G>A
ENST00000643187.1:c.814-174G>A	ENSP00000493507.1:n.814-174G>A
ENST00000674534.1:n.394G>A
ENST00000675467.1:n.3621-174G>A
ENST00000675786.1:c.814-174G>A	ENSP00000502323.1:n.814-174G>A
ENST00000263967.3:c.814-174G>A	ENSP00000263967.3:n.814-174G>A
NM_006218.2:c.814-174G>A , LRG_310t1:c.814-174G>A	NP_006209.2:n.814-174G>A
XM_006713658.2:c.814-174G>A	XP_006713721.1:n.814-174G>A
XM_011512894.1:c.814-174G>A	XP_011511196.1:n.814-174G>A
NM_006218.3:c.814-174G>A	NP_006209.2:n.814-174G>A
XM_006713658.4:c.814-174G>A	XP_006713721.1:n.814-174G>A
XM_011512894.2:c.814-174G>A	XP_011511196.1:n.814-174G>A
NM_006218.4:c.814-174G>A MANE Select	NP_006209.2:n.814-174G>A