Canonical Allele Identifier: CA547913299

Gene: PIK3CA

Linked Data

• gnomAD v2: 3-178921629-CT-C
• gnomAD v4: 3-179203841-CT-C
• MyVariant Identifiers: chr3:g.178921630del (hg19) ; chr3:g.179203842del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203846del , CM000665.2:g.179203846del	GRCh38
NC_000003.11:g.178921634del , CM000665.1:g.178921634del	GRCh37
NC_000003.10:g.180404328del	NCBI36
NG_012113.2:g.60324del , LRG_310:g.60324del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1059+57del MANE Select	ENSP00000263967.3:n.1059+57del
ENST00000643187.1:c.1059+57del	ENSP00000493507.1:n.1059+57del
ENST00000674534.1:n.813+57del
ENST00000675467.1:n.3866+57del
ENST00000675786.1:c.1059+57del	ENSP00000502323.1:n.1059+57del
ENST00000263967.3:c.1059+57del	ENSP00000263967.3:n.1059+57del
NM_006218.2:c.1059+57del , LRG_310t1:c.1059+57del	NP_006209.2:n.1059+57del
XM_006713658.2:c.1059+57del	XP_006713721.1:n.1059+57del
XM_011512894.1:c.1059+57del	XP_011511196.1:n.1059+57del
NM_006218.3:c.1059+57del	NP_006209.2:n.1059+57del
XM_006713658.4:c.1059+57del	XP_006713721.1:n.1059+57del
XM_011512894.2:c.1059+57del	XP_011511196.1:n.1059+57del
NM_006218.4:c.1059+57del MANE Select	NP_006209.2:n.1059+57del