Canonical Allele Identifier: CA1423674680

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219652A= , CM000665.2:g.179219652A=	GRCh38
NC_000003.11:g.178937440A= , CM000665.1:g.178937440A=	GRCh37
NC_000003.10:g.180420134A=	NCBI36
NG_012113.2:g.76130A= , LRG_310:g.76130A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1828A= MANE Select	ENSP00000263967.3:p.Met610=
ENST00000462255.2:n.290A=
ENST00000643187.1:c.1828A=	ENSP00000493507.1:p.Met610=
ENST00000674534.1:n.2736A=
ENST00000674622.1:c.249A=	ENSP00000502417.1:n.249A=
ENST00000675467.1:n.4635A=
ENST00000675786.1:c.*395A=	ENSP00000502323.1:n.*395A=
ENST00000263967.3:c.1828A=	ENSP00000263967.3:p.Met610=
ENST00000462255.1:n.102A=
NM_006218.2:c.1828A= , LRG_310t1:c.1828A=	NP_006209.2:p.Met610=
XM_006713658.2:c.1828A=	XP_006713721.1:p.Met610=
XM_011512894.1:c.1828A=	XP_011511196.1:p.Met610=
NM_006218.3:c.1828A=	NP_006209.2:p.Met610=
XM_006713658.4:c.1828A=	XP_006713721.1:p.Met610=
XM_011512894.2:c.1828A=	XP_011511196.1:p.Met610=
NM_006218.4:c.1828A= MANE Select	NP_006209.2:p.Met610=