Canonical Allele Identifier: CA1423665948

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203949C= , CM000665.2:g.179203949C=	GRCh38
NC_000003.11:g.178921737C= , CM000665.1:g.178921737C=	GRCh37
NC_000003.10:g.180404431C=	NCBI36
NG_012113.2:g.60427C= , LRG_310:g.60427C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1059+160C= MANE Select	ENSP00000263967.3:n.1059+160C=
ENST00000643187.1:c.1059+160C=	ENSP00000493507.1:n.1059+160C=
ENST00000674534.1:n.813+160C=
ENST00000675467.1:n.3866+160C=
ENST00000675786.1:c.1059+160C=	ENSP00000502323.1:n.1059+160C=
ENST00000263967.3:c.1059+160C=	ENSP00000263967.3:n.1059+160C=
NM_006218.2:c.1059+160C= , LRG_310t1:c.1059+160C=	NP_006209.2:n.1059+160C=
XM_006713658.2:c.1059+160C=	XP_006713721.1:n.1059+160C=
XM_011512894.1:c.1059+160C=	XP_011511196.1:n.1059+160C=
NM_006218.3:c.1059+160C=	NP_006209.2:n.1059+160C=
XM_006713658.4:c.1059+160C=	XP_006713721.1:n.1059+160C=
XM_011512894.2:c.1059+160C=	XP_011511196.1:n.1059+160C=
NM_006218.4:c.1059+160C= MANE Select	NP_006209.2:n.1059+160C=