Canonical Allele Identifier: CA2668599357

Gene: PIK3CA

Linked Data

• gnomAD v4: 3-179234376-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234376A>G , CM000665.2:g.179234376A>G	GRCh38
NC_000003.11:g.178952164A>G , CM000665.1:g.178952164A>G	GRCh37
NC_000003.10:g.180434858A>G	NCBI36
NG_012113.2:g.90854A>G , LRG_310:g.90854A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.*12A>G MANE Select	ENSP00000263967.3:n.*12A>G
ENST00000462255.2:n.2242A>G
ENST00000643187.1:c.*299A>G	ENSP00000493507.1:n.*299A>G
ENST00000674534.1:n.4127A>G
ENST00000674622.1:c.1640A>G	ENSP00000502417.1:n.1640A>G
ENST00000675467.1:n.6026A>G
ENST00000675786.1:c.*1786A>G	ENSP00000502323.1:n.*1786A>G
ENST00000675796.1:n.3114A>G
ENST00000263967.3:c.*12A>G	ENSP00000263967.3:n.*12A>G
NM_006218.2:c.*12A>G , LRG_310t1:c.*12A>G	NP_006209.2:n.*12A>G
XM_006713658.2:c.*12A>G	XP_006713721.1:n.*12A>G
XM_011512894.1:c.*12A>G	XP_011511196.1:n.*12A>G
NM_006218.3:c.*12A>G	NP_006209.2:n.*12A>G
XM_006713658.4:c.*12A>G	XP_006713721.1:n.*12A>G
XM_011512894.2:c.*12A>G	XP_011511196.1:n.*12A>G
NM_006218.4:c.*12A>G MANE Select	NP_006209.2:n.*12A>G