Canonical Allele Identifier: CA1423664717

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1724329838
• gnomAD v4: 3-179198736-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179198738del , CM000665.2:g.179198738del	GRCh38
NC_000003.11:g.178916526del , CM000665.1:g.178916526del	GRCh37
NC_000003.10:g.180399220del	NCBI36
NG_012113.2:g.55216del , LRG_310:g.55216del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.-76-12del MANE Select	ENSP00000263967.3:n.-76-12del
ENST00000643187.1:c.-76-12del	ENSP00000493507.1:n.-76-12del
ENST00000675467.1:n.2720del
ENST00000675786.1:c.-76-12del	ENSP00000502323.1:n.-76-12del
ENST00000263967.3:c.-76-12del	ENSP00000263967.3:n.-76-12del
ENST00000468036.1:c.-76-12del	ENSP00000417479.1:n.-76-12del
ENST00000477735.1:c.-76-12del	ENSP00000418145.1:n.-76-12del
NM_006218.2:c.-76-12del , LRG_310t1:c.-76-12del	NP_006209.2:n.-76-12del
XM_006713658.2:c.-76-12del	XP_006713721.1:n.-76-12del
XM_011512894.1:c.-76-12del	XP_011511196.1:n.-76-12del
NM_006218.3:c.-76-12del	NP_006209.2:n.-76-12del
XM_006713658.4:c.-76-12del	XP_006713721.1:n.-76-12del
XM_011512894.2:c.-76-12del	XP_011511196.1:n.-76-12del
NM_006218.4:c.-76-12del MANE Select	NP_006209.2:n.-76-12del