Canonical Allele Identifier: CA437315944

Gene: PIK3CA

Linked Data

• MyVariant Identifiers: chr3:g.178921454C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203666C>A , CM000665.2:g.179203666C>A	GRCh38
NC_000003.11:g.178921454C>A , CM000665.1:g.178921454C>A	GRCh37
NC_000003.10:g.180404148C>A	NCBI36
NG_012113.2:g.60144C>A , LRG_310:g.60144C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.936C>A MANE Select	ENSP00000263967.3:p.Ser312=
ENST00000643187.1:c.936C>A	ENSP00000493507.1:p.Ser312=
ENST00000674534.1:n.690C>A
ENST00000675467.1:n.3743C>A
ENST00000675786.1:c.936C>A	ENSP00000502323.1:p.Ser312=
ENST00000263967.3:c.936C>A	ENSP00000263967.3:p.Ser312=
NM_006218.2:c.936C>A , LRG_310t1:c.936C>A	NP_006209.2:p.Ser312=
XM_006713658.2:c.936C>A	XP_006713721.1:p.Ser312=
XM_011512894.1:c.936C>A	XP_011511196.1:p.Ser312=
NM_006218.3:c.936C>A	NP_006209.2:p.Ser312=
XM_006713658.4:c.936C>A	XP_006713721.1:p.Ser312=
XM_011512894.2:c.936C>A	XP_011511196.1:p.Ser312=
NM_006218.4:c.936C>A MANE Select	NP_006209.2:p.Ser312=