Canonical Allele Identifier: CA2704635413

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108384864

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179198805A>T , CM000665.2:g.179198805A>T	GRCh38
NC_000003.11:g.178916593A>T , CM000665.1:g.178916593A>T	GRCh37
NC_000003.10:g.180399287A>T	NCBI36
NG_012113.2:g.55283A>T , LRG_310:g.55283A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.-21A>T MANE Select	ENSP00000263967.3:n.-21A>T
ENST00000643187.1:c.-21A>T	ENSP00000493507.1:n.-21A>T
ENST00000675467.1:n.2787A>T
ENST00000675786.1:c.-21A>T	ENSP00000502323.1:n.-21A>T
ENST00000263967.3:c.-21A>T	ENSP00000263967.3:n.-21A>T
ENST00000468036.1:c.-21A>T	ENSP00000417479.1:n.-21A>T
ENST00000477735.1:c.-21A>T	ENSP00000418145.1:n.-21A>T
NM_006218.2:c.-21A>T , LRG_310t1:c.-21A>T	NP_006209.2:n.-21A>T
XM_006713658.2:c.-21A>T	XP_006713721.1:n.-21A>T
XM_011512894.1:c.-21A>T	XP_011511196.1:n.-21A>T
NM_006218.3:c.-21A>T	NP_006209.2:n.-21A>T
XM_006713658.4:c.-21A>T	XP_006713721.1:n.-21A>T
XM_011512894.2:c.-21A>T	XP_011511196.1:n.-21A>T
NM_006218.4:c.-21A>T MANE Select	NP_006209.2:n.-21A>T