Canonical Allele Identifier: CA437038940

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1392256153
• gnomAD v3: 3-179234265-G-A
• gnomAD v4: 3-179234265-G-A
• MyVariant Identifiers: chr3:g.178952053G>A (hg19) ; chr3:g.179234265G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234265G>A , CM000665.2:g.179234265G>A	GRCh38
NC_000003.11:g.178952053G>A , CM000665.1:g.178952053G>A	GRCh37
NC_000003.10:g.180434747G>A	NCBI36
NG_012113.2:g.90743G>A , LRG_310:g.90743G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3108G>A MANE Select	ENSP00000263967.3:p.Leu1036=
ENST00000462255.2:n.2131G>A
ENST00000643187.1:c.*188G>A	ENSP00000493507.1:n.*188G>A
ENST00000674534.1:n.4016G>A
ENST00000674622.1:c.1529G>A	ENSP00000502417.1:n.1529G>A
ENST00000675467.1:n.5915G>A
ENST00000675786.1:c.*1675G>A	ENSP00000502323.1:n.*1675G>A
ENST00000675796.1:n.3003G>A
ENST00000263967.3:c.3108G>A	ENSP00000263967.3:p.Leu1036=
NM_006218.2:c.3108G>A , LRG_310t1:c.3108G>A	NP_006209.2:p.Leu1036=
XM_006713658.2:c.3108G>A	XP_006713721.1:p.Leu1036=
XM_011512894.1:c.3108G>A	XP_011511196.1:p.Leu1036=
NM_006218.3:c.3108G>A	NP_006209.2:p.Leu1036=
XM_006713658.4:c.3108G>A	XP_006713721.1:p.Leu1036=
XM_011512894.2:c.3108G>A	XP_011511196.1:p.Leu1036=
NM_006218.4:c.3108G>A MANE Select	NP_006209.2:p.Leu1036=