Canonical Allele Identifier: CA2668622776

Gene: PIK3CA

Linked Data

• gnomAD v4: 3-179219566-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219566C>A , CM000665.2:g.179219566C>A	GRCh38
NC_000003.11:g.178937354C>A , CM000665.1:g.178937354C>A	GRCh37
NC_000003.10:g.180420048C>A	NCBI36
NG_012113.2:g.76044C>A , LRG_310:g.76044C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1747-5C>A MANE Select	ENSP00000263967.3:n.1747-5C>A
ENST00000462255.2:n.209-5C>A
ENST00000643187.1:c.1747-5C>A	ENSP00000493507.1:n.1747-5C>A
ENST00000674534.1:n.2650C>A
ENST00000674622.1:c.168-5C>A	ENSP00000502417.1:n.168-5C>A
ENST00000675467.1:n.4554-5C>A
ENST00000675786.1:c.*314-5C>A	ENSP00000502323.1:n.*314-5C>A
ENST00000263967.3:c.1747-5C>A	ENSP00000263967.3:n.1747-5C>A
ENST00000462255.1:n.16C>A
NM_006218.2:c.1747-5C>A , LRG_310t1:c.1747-5C>A	NP_006209.2:n.1747-5C>A
XM_006713658.2:c.1747-5C>A	XP_006713721.1:n.1747-5C>A
XM_011512894.1:c.1747-5C>A	XP_011511196.1:n.1747-5C>A
NM_006218.3:c.1747-5C>A	NP_006209.2:n.1747-5C>A
XM_006713658.4:c.1747-5C>A	XP_006713721.1:n.1747-5C>A
XM_011512894.2:c.1747-5C>A	XP_011511196.1:n.1747-5C>A
NM_006218.4:c.1747-5C>A MANE Select	NP_006209.2:n.1747-5C>A