Canonical Allele Identifier: CA437315883

Gene: PIK3CA

Linked Data

• gnomAD v4: 3-179203615-T-G
• MyVariant Identifiers: chr3:g.178921403T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203615T>G , CM000665.2:g.179203615T>G	GRCh38
NC_000003.11:g.178921403T>G , CM000665.1:g.178921403T>G	GRCh37
NC_000003.10:g.180404097T>G	NCBI36
NG_012113.2:g.60093T>G , LRG_310:g.60093T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.885T>G MANE Select	ENSP00000263967.3:p.Ser295=
ENST00000643187.1:c.885T>G	ENSP00000493507.1:p.Ser295=
ENST00000674534.1:n.639T>G
ENST00000675467.1:n.3692T>G
ENST00000675786.1:c.885T>G	ENSP00000502323.1:p.Ser295=
ENST00000263967.3:c.885T>G	ENSP00000263967.3:p.Ser295=
NM_006218.2:c.885T>G , LRG_310t1:c.885T>G	NP_006209.2:p.Ser295=
XM_006713658.2:c.885T>G	XP_006713721.1:p.Ser295=
XM_011512894.1:c.885T>G	XP_011511196.1:p.Ser295=
NM_006218.3:c.885T>G	NP_006209.2:p.Ser295=
XM_006713658.4:c.885T>G	XP_006713721.1:p.Ser295=
XM_011512894.2:c.885T>G	XP_011511196.1:p.Ser295=
NM_006218.4:c.885T>G MANE Select	NP_006209.2:p.Ser295=