Canonical Allele Identifier: CA2704386038

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1441647481

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219568C>G , CM000665.2:g.179219568C>G	GRCh38
NC_000003.11:g.178937356C>G , CM000665.1:g.178937356C>G	GRCh37
NC_000003.10:g.180420050C>G	NCBI36
NG_012113.2:g.76046C>G , LRG_310:g.76046C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1747-3C>G MANE Select	ENSP00000263967.3:n.1747-3C>G
ENST00000462255.2:n.209-3C>G
ENST00000643187.1:c.1747-3C>G	ENSP00000493507.1:n.1747-3C>G
ENST00000674534.1:n.2652C>G
ENST00000674622.1:c.168-3C>G	ENSP00000502417.1:n.168-3C>G
ENST00000675467.1:n.4554-3C>G
ENST00000675786.1:c.*314-3C>G	ENSP00000502323.1:n.*314-3C>G
ENST00000263967.3:c.1747-3C>G	ENSP00000263967.3:n.1747-3C>G
ENST00000462255.1:n.18C>G
NM_006218.2:c.1747-3C>G , LRG_310t1:c.1747-3C>G	NP_006209.2:n.1747-3C>G
XM_006713658.2:c.1747-3C>G	XP_006713721.1:n.1747-3C>G
XM_011512894.1:c.1747-3C>G	XP_011511196.1:n.1747-3C>G
NM_006218.3:c.1747-3C>G	NP_006209.2:n.1747-3C>G
XM_006713658.4:c.1747-3C>G	XP_006713721.1:n.1747-3C>G
XM_011512894.2:c.1747-3C>G	XP_011511196.1:n.1747-3C>G
NM_006218.4:c.1747-3C>G MANE Select	NP_006209.2:n.1747-3C>G