Canonical Allele Identifier: CA2704635284

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108384842

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179198799_179198800del , CM000665.2:g.179198799_179198800del	GRCh38
NC_000003.11:g.178916587_178916588del , CM000665.1:g.178916587_178916588del	GRCh37
NC_000003.10:g.180399281_180399282del	NCBI36
NG_012113.2:g.55277_55278del , LRG_310:g.55277_55278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.-27_-26del MANE Select	ENSP00000263967.3:n.-27_-26del
ENST00000643187.1:c.-27_-26del	ENSP00000493507.1:n.-27_-26del
ENST00000675467.1:n.2781_2782del
ENST00000675786.1:c.-27_-26del	ENSP00000502323.1:n.-27_-26del
ENST00000263967.3:c.-27_-26del	ENSP00000263967.3:n.-27_-26del
ENST00000468036.1:c.-27_-26del	ENSP00000417479.1:n.-27_-26del
ENST00000477735.1:c.-27_-26del	ENSP00000418145.1:n.-27_-26del
NM_006218.2:c.-27_-26del , LRG_310t1:c.-27_-26del	NP_006209.2:n.-27_-26del
XM_006713658.2:c.-27_-26del	XP_006713721.1:n.-27_-26del
XM_011512894.1:c.-27_-26del	XP_011511196.1:n.-27_-26del
NM_006218.3:c.-27_-26del	NP_006209.2:n.-27_-26del
XM_006713658.4:c.-27_-26del	XP_006713721.1:n.-27_-26del
XM_011512894.2:c.-27_-26del	XP_011511196.1:n.-27_-26del
NM_006218.4:c.-27_-26del MANE Select	NP_006209.2:n.-27_-26del